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esv2764116

  • Variant Calls:26
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,660

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 547 SVs from 87 studies. See in: genome view    
Remapped(Score: Perfect):15,542,279-15,555,938Question Mark
Overlapping variant regions from other studies: 547 SVs from 87 studies. See in: genome view    
Remapped(Score: Perfect):15,399,788-15,413,447Question Mark
Overlapping variant regions from other studies: 238 SVs from 26 studies. See in: genome view    
Submitted genomic15,444,159-15,457,818Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2764116RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr815,542,27915,555,938
esv2764116RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr815,399,78815,413,447
esv2764116Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000008.9Chr815,444,15915,457,818

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv6992716copy number lossSW_1027SNP arraySNP genotyping analysis33
essv6992717copy number lossSW_1179SNP arraySNP genotyping analysis26
essv6992718copy number lossSW_1447SNP arraySNP genotyping analysis35
essv6992719copy number lossSW_1365SNP arraySNP genotyping analysis36
essv6992720copy number lossSW_0021SNP arraySNP genotyping analysis39
essv6992721copy number lossSW_0033SNP arraySNP genotyping analysis39
essv6992723copy number lossSW_0085SNP arraySNP genotyping analysis42
essv6992724copy number lossSW_0086SNP arraySNP genotyping analysis50
essv6992725copy number lossSW_0183SNP arraySNP genotyping analysis45
essv6992726copy number lossSW_0191SNP arraySNP genotyping analysis36
essv6992727copy number lossSW_0241SNP arraySNP genotyping analysis45
essv6992728copy number lossSW_0341SNP arraySNP genotyping analysis25
essv6992729copy number lossSW_0552SNP arraySNP genotyping analysis42
essv6992730copy number lossSW_0653SNP arraySNP genotyping analysis37
essv6992731copy number lossSW_0659SNP arraySNP genotyping analysis35
essv6992732copy number lossSW_0759SNP arraySNP genotyping analysis44
essv6992734copy number lossSW_0815SNP arraySNP genotyping analysis46
essv6992735copy number lossSW_1103SNP arraySNP genotyping analysis43
essv6992736copy number lossSW_1116SNP arraySNP genotyping analysis50
essv6992737copy number lossSW_1209SNP arraySNP genotyping analysis45
essv6992738copy number lossSW_1323SNP arraySNP genotyping analysis29
essv6992739copy number lossSW_1346SNP arraySNP genotyping analysis42
essv6992740copy number lossSW_1409SNP arraySNP genotyping analysis40
essv6992741copy number lossSW_1451SNP arraySNP genotyping analysis26
essv6992742copy number lossSW_1527SNP arraySNP genotyping analysis33
essv6992743copy number lossSW_1551SNP arraySNP genotyping analysis22

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv6992716RemappedPerfectNC_000008.11:g.(?_
15542279)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,542,27915,555,938
essv6992717RemappedPerfectNC_000008.11:g.(?_
15542279)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,542,27915,555,938
essv6992718RemappedPerfectNC_000008.11:g.(?_
15542279)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,542,27915,555,938
essv6992719RemappedPerfectNC_000008.11:g.(?_
15543669)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,543,66915,555,938
essv6992720RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992721RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992723RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992724RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992725RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992726RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992727RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992728RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992729RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992730RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992731RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992732RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992734RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992735RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992736RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992737RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992738RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992739RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992740RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992741RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992742RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992743RemappedPerfectNC_000008.11:g.(?_
15545551)_(1555593
8_?)del
GRCh38.p12First PassNC_000008.11Chr815,545,55115,555,938
essv6992716RemappedPerfectNC_000008.10:g.(?_
15399788)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,399,78815,413,447
essv6992717RemappedPerfectNC_000008.10:g.(?_
15399788)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,399,78815,413,447
essv6992718RemappedPerfectNC_000008.10:g.(?_
15399788)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,399,78815,413,447
essv6992719RemappedPerfectNC_000008.10:g.(?_
15401178)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,401,17815,413,447
essv6992720RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992721RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992723RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992724RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992725RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992726RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992727RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992728RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992729RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992730RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992731RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992732RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992734RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992735RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992736RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992737RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992738RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992739RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992740RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992741RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992742RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992743RemappedPerfectNC_000008.10:g.(?_
15403060)_(1541344
7_?)del
GRCh37.p13First PassNC_000008.10Chr815,403,06015,413,447
essv6992716Submitted genomicNC_000008.9:g.(?_1
5444159)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,444,15915,457,818
essv6992717Submitted genomicNC_000008.9:g.(?_1
5444159)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,444,15915,457,818
essv6992718Submitted genomicNC_000008.9:g.(?_1
5444159)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,444,15915,457,818
essv6992719Submitted genomicNC_000008.9:g.(?_1
5445549)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,445,54915,457,818
essv6992720Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992721Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992723Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992724Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992725Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992726Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992727Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992728Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992729Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992730Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992731Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992732Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992734Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992735Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992736Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992737Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992738Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992739Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992740Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992741Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992742Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818
essv6992743Submitted genomicNC_000008.9:g.(?_1
5447431)_(15457818
_?)del
NCBI36 (hg18)NC_000008.9Chr815,447,43115,457,818

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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