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esv2757685

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:422,609

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1553 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):71,881,805-72,304,413Question Mark
Overlapping variant regions from other studies: 1553 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):69,549,041-69,971,648Question Mark
Overlapping variant regions from other studies: 113 SVs from 8 studies. See in: genome view    
Submitted genomic67,700,021-68,122,628Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2757685RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1871,881,80572,304,413
esv2757685RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1869,549,04169,971,648
esv2757685Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000018.8Chr1867,700,02168,122,628

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv2914copy number lossNA19007SNP arraySNP genotyping analysis106

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv2914RemappedPerfectNC_000018.10:g.(71
881805_71881805)_(
72304413_72304413)
del
GRCh38.p12First PassNC_000018.10Chr1871,881,80571,881,80572,304,41372,304,413
essv2914RemappedPerfectNC_000018.9:g.(695
49041_69587022)_(6
9882429_69971648)d
el
GRCh37.p13First PassNC_000018.9Chr1869,549,04169,587,02269,882,42969,971,648
essv2914Submitted genomicNC_000018.8:g.(677
00021_67738002)_(6
8033409_68122628)d
el
NCBI35 (hg17)NC_000018.8Chr1867,700,02167,738,00268,033,40968,122,628

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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