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esv2757473

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:179,678

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 686 SVs from 76 studies. See in: genome view    
Remapped(Score: Good):103,165,062-103,344,739Question Mark
Overlapping variant regions from other studies: 686 SVs from 76 studies. See in: genome view    
Remapped(Score: Perfect):103,035,791-103,215,467Question Mark
Overlapping variant regions from other studies: 38 SVs from 7 studies. See in: genome view    
Submitted genomic102,541,001-102,720,677Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2757473RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11103,165,062103,344,739
esv2757473RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11103,035,791103,215,467
esv2757473Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000011.8Chr11102,541,001102,720,677

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5763copy number lossNA18540SNP arraySNP genotyping analysis75

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv5763RemappedGoodNC_000011.10:g.(10
3165062_103165062)
_(103344739_103344
739)del
GRCh38.p12First PassNC_000011.10Chr11103,165,062103,165,062103,344,739103,344,739
essv5763RemappedPerfectNC_000011.9:g.(103
035791_103067460)_
(103215467_1032154
67)del
GRCh37.p13First PassNC_000011.9Chr11103,035,791103,067,460103,215,467103,215,467
essv5763Submitted genomicNC_000011.8:g.(102
541001_102572670)_
(102720677_1027206
77)del
NCBI35 (hg17)NC_000011.8Chr11102,541,001102,572,670102,720,677102,720,677

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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