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nsv5857592

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,741

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 155 SVs from 41 studies. See in: genome view    
Submitted genomic4,587,191-4,592,931Question Mark
Overlapping variant regions from other studies: 155 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):4,608,421-4,614,161Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5857592Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr114,587,1914,592,931
nsv5857592RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr114,608,4214,614,161

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17453565copy number variationSequencingSequence alignment4
nssv17457824copy number variationSequencingSequence alignment3

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17453565Submitted genomicGRCh38 (hg38)NC_000011.10Chr114,587,1914,592,931
nssv17457824Submitted genomicGRCh38 (hg38)NC_000011.10Chr114,587,1914,592,931
nssv17453565RemappedPerfectGRCh37.p13First PassNC_000011.9Chr114,608,4214,614,161
nssv17457824RemappedPerfectGRCh37.p13First PassNC_000011.9Chr114,608,4214,614,161

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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