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nsv5830714

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,149

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 270 SVs from 56 studies. See in: genome view    
Submitted genomic61,973,166-61,983,314Question Mark
Overlapping variant regions from other studies: 270 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):62,438,838-62,448,986Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5830714Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr161,973,16661,983,314
nsv5830714RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr162,438,83862,448,986

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17480139copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17480139Submitted genomicGRCh38 (hg38)NC_000001.11Chr161,973,16661,983,314
nssv17480139RemappedPerfectGRCh37.p13First PassNC_000001.10Chr162,438,83862,448,986

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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