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nsv5610396

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
Submitted genomic116,986,977-116,986,977Question Mark
Overlapping variant regions from other studies: 126 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):117,529,599-117,529,599Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5610396Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1116,986,977116,986,977
nsv5610396RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1117,529,599117,529,599

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17059796insertionHG02587SequencingSequence alignment2,330

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17059796Submitted genomicNC_000001.11:g.116
986977_116986978in
s499
GRCh38 (hg38)NC_000001.11Chr1116,986,977116,986,977
nssv17059796RemappedPerfectNC_000001.10:g.117
529599_117529600in
s499
GRCh37.p13First PassNC_000001.10Chr1117,529,599117,529,599

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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