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nsv5213628

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,100

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 216 SVs from 42 studies. See in: genome view    
Submitted genomic625,601-629,700Question Mark
Overlapping variant regions from other studies: 223 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):560,981-565,080Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5213628Submitted genomicGRCh38.p13Primary AssemblyNC_000001.11Chr1625,601629,700
nsv5213628RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1560,981565,080

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16831823copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16831823Submitted genomicGRCh38.p13NC_000001.11Chr1625,601629,700
nssv16831823RemappedPerfectGRCh37.p13First PassNC_000001.10Chr1560,981565,080

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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