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nsv5295751

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,668

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 264 SVs from 45 studies. See in: genome view    
Submitted genomic27,856,477-27,885,144Question Mark
Overlapping variant regions from other studies: 264 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):28,347,385-28,376,052Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5295751Submitted genomicGRCh38.p13Primary AssemblyNC_000019.10Chr1927,856,47727,885,144
nsv5295751RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1928,347,38528,376,052

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16786867copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16786867Submitted genomicGRCh38.p13NC_000019.10Chr1927,856,47727,885,144
nssv16786867RemappedPerfectGRCh37.p13First PassNC_000019.9Chr1928,347,38528,376,052

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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