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nsv5834585

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,100

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 116 SVs from 24 studies. See in: genome view    
Submitted genomic127,696,739-127,697,838Question Mark
Overlapping variant regions from other studies: 116 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):127,415,582-127,416,681Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5834585Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3127,696,739127,697,838
nsv5834585RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3127,415,582127,416,681

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17484460copy number variationSequencingSequence alignment0

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17484460Submitted genomicGRCh38 (hg38)NC_000003.12Chr3127,696,739127,697,838
nssv17484460RemappedPerfectGRCh37.p13First PassNC_000003.11Chr3127,415,582127,416,681

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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