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nsv5873011

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,811

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 122 SVs from 22 studies. See in: genome view    
Submitted genomic71,137,216-71,143,026Question Mark
Overlapping variant regions from other studies: 122 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):69,133,357-69,139,167Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5873011Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1771,137,21671,143,026
nsv5873011RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1769,133,35769,139,167

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17475877copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17475877Submitted genomicGRCh38 (hg38)NC_000017.11Chr1771,137,21671,143,026
nssv17475877RemappedPerfectGRCh37.p13First PassNC_000017.10Chr1769,133,35769,139,167

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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