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nsv1141769

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:159

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 142 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):57,687,494-57,687,652Question Mark
Overlapping variant regions from other studies: 142 SVs from 36 studies. See in: genome view    
Submitted genomic57,979,692-57,979,850Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv1141769RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1557,687,49457,687,652
nsv1141769Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000015.9Chr1557,979,69257,979,850

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv3993275insertionKWS2SequencingRead depth and paired-end mapping21,718

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv3993275RemappedPerfectNC_000015.10:g.(57
687494_?)_(?_57687
652)ins?
GRCh38.p12First PassNC_000015.10Chr1557,687,49457,687,652
nssv3993275Submitted genomicNC_000015.9:g.(579
79692_?)_(?_579798
50)ins?
GRCh37 (hg19)NC_000015.9Chr1557,979,69257,979,850

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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