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nsv1077919

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:122,702

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1508 SVs from 76 studies. See in: genome view    
Remapped(Score: Perfect):10,619,157-10,741,858Question Mark
Overlapping variant regions from other studies: 1471 SVs from 80 studies. See in: genome view    
Submitted genomic10,770,599-10,893,300Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv1077919RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000021.9Chr2110,619,15710,741,858
nsv1077919Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000021.8Chr2110,770,59910,893,300

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv3763959duplicationKWP1SequencingRead depth and paired-end mapping11,116

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv3763959RemappedPerfectNC_000021.9:g.1061
9157_10741858dup
GRCh38.p12First PassNC_000021.9Chr2110,619,15710,741,858
nssv3763959Submitted genomicNC_000021.8:g.1077
0599_10893300dup
GRCh37 (hg19)NC_000021.8Chr2110,770,59910,893,300

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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