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esv20564

  • Variant Calls:21
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:57,769

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 455 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):37,148,725-37,206,493Question Mark
Overlapping variant regions from other studies: 455 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):37,437,653-37,495,421Question Mark
Overlapping variant regions from other studies: 156 SVs from 22 studies. See in: genome view    
Submitted genomic37,477,659-37,535,427Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv20564RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1037,148,72537,206,493
esv20564RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1037,437,65337,495,421
esv20564Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000010.9Chr1037,477,65937,535,427

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv52017copy number lossNA12006Oligo aCGHProbe signal intensity1,080
essv33095copy number lossNA19147Oligo aCGHProbe signal intensity1,541
essv79812copy number lossNA12749Oligo aCGHProbe signal intensity1,232
essv57245copy number lossNA11993Oligo aCGHProbe signal intensity1,116
essv48366copy number lossNA07037Oligo aCGHProbe signal intensity1,154
essv43153copy number lossNA18909Oligo aCGHProbe signal intensity1,535
essv80023copy number lossNA11995Oligo aCGHProbe signal intensity1,228
essv68205copy number gainNA18858Oligo aCGHProbe signal intensity1,507
essv41898copy number gainNA18505Oligo aCGHProbe signal intensity1,411
essv46691copy number gainNA19129Oligo aCGHProbe signal intensity1,564
essv63315copy number lossNA15510Oligo aCGHProbe signal intensity1,307
essv74672copy number lossNA12004Oligo aCGHProbe signal intensity1,123
essv73290copy number lossNA12156Oligo aCGHProbe signal intensity1,085
essv56507copy number gainNA12776Oligo aCGHProbe signal intensity1,114
essv39972copy number lossNA12878Oligo aCGHProbe signal intensity1,172
essv50996copy number lossNA11931Oligo aCGHProbe signal intensity1,027
essv45151copy number lossNA12489Oligo aCGHProbe signal intensity1,098
essv61443copy number lossNA12239Oligo aCGHProbe signal intensity1,252
essv64658copy number lossNA07045Oligo aCGHProbe signal intensity1,341
essv36965copy number lossNA11894Oligo aCGHProbe signal intensity1,114
essv81496copy number lossNA19114Oligo aCGHProbe signal intensity1,473

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv52017RemappedPerfectNC_000010.11:g.(?_
37148387)_(3719787
8_?)del
GRCh38.p12First PassNC_000010.11Chr1037,148,38737,197,878
essv33095RemappedPerfectNC_000010.11:g.(?_
37148387)_(3720185
4_?)del
GRCh38.p12First PassNC_000010.11Chr1037,148,38737,201,854
essv79812RemappedPerfectNC_000010.11:g.(?_
37148725)_(3719792
9_?)del
GRCh38.p12First PassNC_000010.11Chr1037,148,72537,197,929
essv57245RemappedPerfectNC_000010.11:g.(?_
37149406)_(3719748
0_?)del
GRCh38.p12First PassNC_000010.11Chr1037,149,40637,197,480
essv48366RemappedPerfectNC_000010.11:g.(?_
37150298)_(3720649
3_?)del
GRCh38.p12First PassNC_000010.11Chr1037,150,29837,206,493
essv43153RemappedPerfectNC_000010.11:g.(?_
37151049)_(3719376
6_?)del
GRCh38.p12First PassNC_000010.11Chr1037,151,04937,193,766
essv80023RemappedPerfectNC_000010.11:g.(?_
37151049)_(3720199
9_?)del
GRCh38.p12First PassNC_000010.11Chr1037,151,04937,201,999
essv68205RemappedPerfectNC_000010.11:g.(?_
37151124)_(3720185
4_?)dup
GRCh38.p12First PassNC_000010.11Chr1037,151,12437,201,854
essv41898RemappedPerfectNC_000010.11:g.(?_
37151124)_(3720684
5_?)dup
GRCh38.p12First PassNC_000010.11Chr1037,151,12437,206,845
essv46691RemappedPerfectNC_000010.11:g.(?_
37157223)_(3719748
0_?)dup
GRCh38.p12First PassNC_000010.11Chr1037,157,22337,197,480
essv63315RemappedPerfectNC_000010.11:g.(?_
37157296)_(3719546
9_?)del
GRCh38.p12First PassNC_000010.11Chr1037,157,29637,195,469
essv74672RemappedPerfectNC_000010.11:g.(?_
37157296)_(3719787
8_?)del
GRCh38.p12First PassNC_000010.11Chr1037,157,29637,197,878
essv73290RemappedPerfectNC_000010.11:g.(?_
37157372)_(3720649
3_?)del
GRCh38.p12First PassNC_000010.11Chr1037,157,37237,206,493
essv56507RemappedPerfectNC_000010.11:g.(?_
37162149)_(3719776
2_?)dup
GRCh38.p12First PassNC_000010.11Chr1037,162,14937,197,762
essv39972RemappedPerfectNC_000010.11:g.(?_
37162214)_(3720696
9_?)del
GRCh38.p12First PassNC_000010.11Chr1037,162,21437,206,969
essv50996RemappedPerfectNC_000010.11:g.(?_
37162730)_(3719846
9_?)del
GRCh38.p12First PassNC_000010.11Chr1037,162,73037,198,469
essv45151RemappedPerfectNC_000010.11:g.(?_
37162730)_(3720096
8_?)del
GRCh38.p12First PassNC_000010.11Chr1037,162,73037,200,968
essv61443RemappedPerfectNC_000010.11:g.(?_
37162869)_(3719787
8_?)del
GRCh38.p12First PassNC_000010.11Chr1037,162,86937,197,878
essv64658RemappedPerfectNC_000010.11:g.(?_
37162990)_(3719748
0_?)del
GRCh38.p12First PassNC_000010.11Chr1037,162,99037,197,480
essv36965RemappedPerfectNC_000010.11:g.(?_
37162990)_(3719831
4_?)del
GRCh38.p12First PassNC_000010.11Chr1037,162,99037,198,314
essv81496RemappedPerfectNC_000010.11:g.(?_
37165491)_(3720053
4_?)del
GRCh38.p12First PassNC_000010.11Chr1037,165,49137,200,534
essv52017RemappedPerfectNC_000010.10:g.(?_
37437315)_(3748680
6_?)del
GRCh37.p13First PassNC_000010.10Chr1037,437,31537,486,806
essv33095RemappedPerfectNC_000010.10:g.(?_
37437315)_(3749078
2_?)del
GRCh37.p13First PassNC_000010.10Chr1037,437,31537,490,782
essv79812RemappedPerfectNC_000010.10:g.(?_
37437653)_(3748685
7_?)del
GRCh37.p13First PassNC_000010.10Chr1037,437,65337,486,857
essv57245RemappedPerfectNC_000010.10:g.(?_
37438334)_(3748640
8_?)del
GRCh37.p13First PassNC_000010.10Chr1037,438,33437,486,408
essv48366RemappedPerfectNC_000010.10:g.(?_
37439226)_(3749542
1_?)del
GRCh37.p13First PassNC_000010.10Chr1037,439,22637,495,421
essv43153RemappedPerfectNC_000010.10:g.(?_
37439977)_(3748269
4_?)del
GRCh37.p13First PassNC_000010.10Chr1037,439,97737,482,694
essv80023RemappedPerfectNC_000010.10:g.(?_
37439977)_(3749092
7_?)del
GRCh37.p13First PassNC_000010.10Chr1037,439,97737,490,927
essv68205RemappedPerfectNC_000010.10:g.(?_
37440052)_(3749078
2_?)dup
GRCh37.p13First PassNC_000010.10Chr1037,440,05237,490,782
essv41898RemappedPerfectNC_000010.10:g.(?_
37440052)_(3749577
3_?)dup
GRCh37.p13First PassNC_000010.10Chr1037,440,05237,495,773
essv46691RemappedPerfectNC_000010.10:g.(?_
37446151)_(3748640
8_?)dup
GRCh37.p13First PassNC_000010.10Chr1037,446,15137,486,408
essv63315RemappedPerfectNC_000010.10:g.(?_
37446224)_(3748439
7_?)del
GRCh37.p13First PassNC_000010.10Chr1037,446,22437,484,397
essv74672RemappedPerfectNC_000010.10:g.(?_
37446224)_(3748680
6_?)del
GRCh37.p13First PassNC_000010.10Chr1037,446,22437,486,806
essv73290RemappedPerfectNC_000010.10:g.(?_
37446300)_(3749542
1_?)del
GRCh37.p13First PassNC_000010.10Chr1037,446,30037,495,421
essv56507RemappedPerfectNC_000010.10:g.(?_
37451077)_(3748669
0_?)dup
GRCh37.p13First PassNC_000010.10Chr1037,451,07737,486,690
essv39972RemappedPerfectNC_000010.10:g.(?_
37451142)_(3749589
7_?)del
GRCh37.p13First PassNC_000010.10Chr1037,451,14237,495,897
essv50996RemappedPerfectNC_000010.10:g.(?_
37451658)_(3748739
7_?)del
GRCh37.p13First PassNC_000010.10Chr1037,451,65837,487,397
essv45151RemappedPerfectNC_000010.10:g.(?_
37451658)_(3748989
6_?)del
GRCh37.p13First PassNC_000010.10Chr1037,451,65837,489,896
essv61443RemappedPerfectNC_000010.10:g.(?_
37451797)_(3748680
6_?)del
GRCh37.p13First PassNC_000010.10Chr1037,451,79737,486,806
essv64658RemappedPerfectNC_000010.10:g.(?_
37451918)_(3748640
8_?)del
GRCh37.p13First PassNC_000010.10Chr1037,451,91837,486,408
essv36965RemappedPerfectNC_000010.10:g.(?_
37451918)_(3748724
2_?)del
GRCh37.p13First PassNC_000010.10Chr1037,451,91837,487,242
essv81496RemappedPerfectNC_000010.10:g.(?_
37454419)_(3748946
2_?)del
GRCh37.p13First PassNC_000010.10Chr1037,454,41937,489,462
essv52017Submitted genomicNC_000010.9:g.(?_3
7477321)_(37526812
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,477,32137,526,812
essv33095Submitted genomicNC_000010.9:g.(?_3
7477321)_(37530788
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,477,32137,530,788
essv79812Submitted genomicNC_000010.9:g.(?_3
7477659)_(37526863
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,477,65937,526,863
essv57245Submitted genomicNC_000010.9:g.(?_3
7478340)_(37526414
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,478,34037,526,414
essv48366Submitted genomicNC_000010.9:g.(?_3
7479232)_(37535427
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,479,23237,535,427
essv43153Submitted genomicNC_000010.9:g.(?_3
7479983)_(37522700
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,479,98337,522,700
essv80023Submitted genomicNC_000010.9:g.(?_3
7479983)_(37530933
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,479,98337,530,933
essv68205Submitted genomicNC_000010.9:g.(?_3
7480058)_(37530788
_?)dup
NCBI36 (hg18)NC_000010.9Chr1037,480,05837,530,788
essv41898Submitted genomicNC_000010.9:g.(?_3
7480058)_(37535779
_?)dup
NCBI36 (hg18)NC_000010.9Chr1037,480,05837,535,779
essv46691Submitted genomicNC_000010.9:g.(?_3
7486157)_(37526414
_?)dup
NCBI36 (hg18)NC_000010.9Chr1037,486,15737,526,414
essv63315Submitted genomicNC_000010.9:g.(?_3
7486230)_(37524403
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,486,23037,524,403
essv74672Submitted genomicNC_000010.9:g.(?_3
7486230)_(37526812
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,486,23037,526,812
essv73290Submitted genomicNC_000010.9:g.(?_3
7486306)_(37535427
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,486,30637,535,427
essv56507Submitted genomicNC_000010.9:g.(?_3
7491083)_(37526696
_?)dup
NCBI36 (hg18)NC_000010.9Chr1037,491,08337,526,696
essv39972Submitted genomicNC_000010.9:g.(?_3
7491148)_(37535903
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,491,14837,535,903
essv50996Submitted genomicNC_000010.9:g.(?_3
7491664)_(37527403
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,491,66437,527,403
essv45151Submitted genomicNC_000010.9:g.(?_3
7491664)_(37529902
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,491,66437,529,902
essv61443Submitted genomicNC_000010.9:g.(?_3
7491803)_(37526812
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,491,80337,526,812
essv64658Submitted genomicNC_000010.9:g.(?_3
7491924)_(37526414
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,491,92437,526,414
essv36965Submitted genomicNC_000010.9:g.(?_3
7491924)_(37527248
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,491,92437,527,248
essv81496Submitted genomicNC_000010.9:g.(?_3
7494425)_(37529468
_?)del
NCBI36 (hg18)NC_000010.9Chr1037,494,42537,529,468

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv483662NA07037Oligo aCGHProbe signal intensityPass
essv646582NA07045Oligo aCGHProbe signal intensityPass
essv369652NA11894Oligo aCGHProbe signal intensityPass
essv509962NA11931Oligo aCGHProbe signal intensityPass
essv572452NA11993Oligo aCGHProbe signal intensityPass
essv800232NA11995Oligo aCGHProbe signal intensityPass
essv746722NA12004Oligo aCGHProbe signal intensityPass
essv520172NA12006Oligo aCGHProbe signal intensityPass
essv732902NA12156Oligo aCGHProbe signal intensityPass
essv614432NA12239Oligo aCGHProbe signal intensityPass
essv451512NA12489Oligo aCGHProbe signal intensityPass
essv798122NA12749Oligo aCGHProbe signal intensityPass
essv565072NA12776Oligo aCGHProbe signal intensityPass
essv399722NA12878Oligo aCGHProbe signal intensityPass
essv633152NA15510Oligo aCGHProbe signal intensityPass
essv418982NA18505Oligo aCGHProbe signal intensityPass
essv682052NA18858Oligo aCGHProbe signal intensityPass
essv431532NA18909Oligo aCGHProbe signal intensityPass
essv814962NA19114Oligo aCGHProbe signal intensityPass
essv466912NA19129Oligo aCGHProbe signal intensityPass
essv330952NA19147Oligo aCGHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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