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esv2762699

  • Variant Calls:44
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,568

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1169 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):69,070,193-69,091,760Question Mark
Overlapping variant regions from other studies: 1169 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):66,737,430-66,758,997Question Mark
Overlapping variant regions from other studies: 600 SVs from 28 studies. See in: genome view    
Submitted genomic64,888,410-64,909,977Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2762699RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1869,070,19369,091,760
esv2762699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1866,737,43066,758,997
esv2762699Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000018.8Chr1864,888,41064,909,977

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7003102copy number lossSW_1092SNP arraySNP genotyping analysis38
essv7003103copy number lossSW_0200SNP arraySNP genotyping analysis51
essv7003104copy number lossSW_1027SNP arraySNP genotyping analysis33
essv7003105copy number lossSW_1253SNP arraySNP genotyping analysis31
essv7003106copy number lossSW_1374SNP arraySNP genotyping analysis28
essv7003107copy number lossSW_1163SNP arraySNP genotyping analysis45
essv7003108copy number lossSW_0651SNP arraySNP genotyping analysis47
essv7003109copy number lossSW_1428SNP arraySNP genotyping analysis37
essv7003110copy number lossSW_1435SNP arraySNP genotyping analysis32
essv7003111copy number lossSW_1346SNP arraySNP genotyping analysis42
essv7003113copy number lossSW_0059SNP arraySNP genotyping analysis36
essv7003114copy number lossSW_0144SNP arraySNP genotyping analysis51
essv7003115copy number lossSW_0159SNP arraySNP genotyping analysis52
essv7003116copy number lossSW_0790SNP arraySNP genotyping analysis48
essv7003117copy number lossSW_0828SNP arraySNP genotyping analysis33
essv7003118copy number lossSW_0861SNP arraySNP genotyping analysis44
essv7003119copy number lossSW_1017SNP arraySNP genotyping analysis33
essv7003120copy number lossSW_1058SNP arraySNP genotyping analysis26
essv7003121copy number lossSW_1078SNP arraySNP genotyping analysis32
essv7003122copy number lossSW_1096SNP arraySNP genotyping analysis38
essv7003124copy number lossSW_1105SNP arraySNP genotyping analysis49
essv7003125copy number lossSW_1113SNP arraySNP genotyping analysis51
essv7003126copy number lossSW_1192SNP arraySNP genotyping analysis29
essv7003127copy number lossSW_1281SNP arraySNP genotyping analysis35
essv7003128copy number lossSW_1365SNP arraySNP genotyping analysis36
essv7003129copy number lossSW_1409SNP arraySNP genotyping analysis40
essv7003130copy number lossSW_1431SNP arraySNP genotyping analysis30
essv7003131copy number lossSW_1437SNP arraySNP genotyping analysis29
essv7003132copy number lossSW_1439SNP arraySNP genotyping analysis34
essv7003133copy number lossSW_1543SNP arraySNP genotyping analysis29
essv7003135copy number lossSW_0211SNP arraySNP genotyping analysis33
essv7003136copy number lossSW_0604SNP arraySNP genotyping analysis48
essv7003137copy number lossSW_1547SNP arraySNP genotyping analysis33
essv7003138copy number lossSW_0883SNP arraySNP genotyping analysis37
essv7003139copy number lossSW_0047SNP arraySNP genotyping analysis42
essv7003140copy number lossSW_0255SNP arraySNP genotyping analysis31
essv7003141copy number lossSW_0641SNP arraySNP genotyping analysis37
essv7003142copy number lossSW_0816SNP arraySNP genotyping analysis31
essv7003143copy number lossSW_0831SNP arraySNP genotyping analysis42
essv7003144copy number lossSW_0859SNP arraySNP genotyping analysis43
essv7003146copy number lossSW_1318SNP arraySNP genotyping analysis38
essv7003147copy number lossSW_0677SNP arraySNP genotyping analysis32
essv7003148copy number lossSW_1063SNP arraySNP genotyping analysis50
essv7003149copy number lossSW_1264SNP arraySNP genotyping analysis33

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7003102RemappedPerfectNC_000018.10:g.(?_
69070193)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,070,19369,086,089
essv7003103RemappedPerfectNC_000018.10:g.(?_
69075039)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,075,03969,086,089
essv7003104RemappedPerfectNC_000018.10:g.(?_
69075039)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,075,03969,086,089
essv7003105RemappedPerfectNC_000018.10:g.(?_
69075039)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,075,03969,086,089
essv7003106RemappedPerfectNC_000018.10:g.(?_
69075039)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,075,03969,086,089
essv7003107RemappedPerfectNC_000018.10:g.(?_
69075039)_(6909055
0_?)del
GRCh38.p12First PassNC_000018.10Chr1869,075,03969,090,550
essv7003108RemappedPerfectNC_000018.10:g.(?_
69075518)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,075,51869,086,089
essv7003109RemappedPerfectNC_000018.10:g.(?_
69075518)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,075,51869,086,089
essv7003110RemappedPerfectNC_000018.10:g.(?_
69075518)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,075,51869,086,089
essv7003111RemappedPerfectNC_000018.10:g.(?_
69075518)_(6909102
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,075,51869,091,029
essv7003113RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003114RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003115RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003116RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003117RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003118RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003119RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003120RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003121RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003122RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003124RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003125RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003126RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003127RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003128RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003129RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003130RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003131RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003132RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003133RemappedPerfectNC_000018.10:g.(?_
69078869)_(6908608
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,086,089
essv7003135RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909055
0_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,090,550
essv7003136RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909055
0_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,090,550
essv7003137RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909055
0_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,090,550
essv7003138RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909093
2_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,090,932
essv7003139RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909102
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,091,029
essv7003140RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909102
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,091,029
essv7003141RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909102
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,091,029
essv7003142RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909102
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,091,029
essv7003143RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909102
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,091,029
essv7003144RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909102
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,091,029
essv7003146RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909102
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,091,029
essv7003147RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909148
4_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,091,484
essv7003148RemappedPerfectNC_000018.10:g.(?_
69078869)_(6909176
0_?)del
GRCh38.p12First PassNC_000018.10Chr1869,078,86969,091,760
essv7003149RemappedPerfectNC_000018.10:g.(?_
69083700)_(6909102
9_?)del
GRCh38.p12First PassNC_000018.10Chr1869,083,70069,091,029
essv7003102RemappedPerfectNC_000018.9:g.(?_6
6737430)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,737,43066,753,326
essv7003103RemappedPerfectNC_000018.9:g.(?_6
6742276)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,742,27666,753,326
essv7003104RemappedPerfectNC_000018.9:g.(?_6
6742276)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,742,27666,753,326
essv7003105RemappedPerfectNC_000018.9:g.(?_6
6742276)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,742,27666,753,326
essv7003106RemappedPerfectNC_000018.9:g.(?_6
6742276)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,742,27666,753,326
essv7003107RemappedPerfectNC_000018.9:g.(?_6
6742276)_(66757787
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,742,27666,757,787
essv7003108RemappedPerfectNC_000018.9:g.(?_6
6742755)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,742,75566,753,326
essv7003109RemappedPerfectNC_000018.9:g.(?_6
6742755)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,742,75566,753,326
essv7003110RemappedPerfectNC_000018.9:g.(?_6
6742755)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,742,75566,753,326
essv7003111RemappedPerfectNC_000018.9:g.(?_6
6742755)_(66758266
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,742,75566,758,266
essv7003113RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003114RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003115RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003116RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003117RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003118RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003119RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003120RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003121RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003122RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003124RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003125RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003126RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003127RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003128RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003129RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003130RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003131RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003132RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003133RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66753326
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,753,326
essv7003135RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66757787
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,757,787
essv7003136RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66757787
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,757,787
essv7003137RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66757787
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,757,787
essv7003138RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66758169
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,758,169
essv7003139RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66758266
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,758,266
essv7003140RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66758266
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,758,266
essv7003141RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66758266
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,758,266
essv7003142RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66758266
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,758,266
essv7003143RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66758266
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,758,266
essv7003144RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66758266
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,758,266
essv7003146RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66758266
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,758,266
essv7003147RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66758721
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,758,721
essv7003148RemappedPerfectNC_000018.9:g.(?_6
6746106)_(66758997
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,746,10666,758,997
essv7003149RemappedPerfectNC_000018.9:g.(?_6
6750937)_(66758266
_?)del
GRCh37.p13First PassNC_000018.9Chr1866,750,93766,758,266
essv7003102Submitted genomicNC_000018.8:g.(?_6
4888410)_(64904306
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,888,41064,904,306
essv7003103Submitted genomicNC_000018.8:g.(?_6
4893256)_(64904306
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,893,25664,904,306
essv7003104Submitted genomicNC_000018.8:g.(?_6
4893256)_(64904306
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,893,25664,904,306
essv7003105Submitted genomicNC_000018.8:g.(?_6
4893256)_(64904306
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,893,25664,904,306
essv7003106Submitted genomicNC_000018.8:g.(?_6
4893256)_(64904306
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,893,25664,904,306
essv7003107Submitted genomicNC_000018.8:g.(?_6
4893256)_(64908767
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,893,25664,908,767
essv7003108Submitted genomicNC_000018.8:g.(?_6
4893735)_(64904306
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,893,73564,904,306
essv7003109Submitted genomicNC_000018.8:g.(?_6
4893735)_(64904306
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,893,73564,904,306
essv7003110Submitted genomicNC_000018.8:g.(?_6
4893735)_(64904306
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,893,73564,904,306
essv7003111Submitted genomicNC_000018.8:g.(?_6
4893735)_(64909246
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,893,73564,909,246
essv7003113Submitted genomicNC_000018.8:g.(?_6
4897086)_(64904306
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,897,08664,904,306
essv7003114Submitted genomicNC_000018.8:g.(?_6
4897086)_(64904306
_?)del
NCBI36 (hg18)NC_000018.8Chr1864,897,08664,904,306
Showing 100 of 132

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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