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nsv5261840

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,652

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 445 SVs from 79 studies. See in: genome view    
Submitted genomic27,494,347-27,501,998Question Mark
Overlapping variant regions from other studies: 445 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):27,647,280-27,654,931Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5261840Submitted genomicGRCh38.p13Primary AssemblyNC_000012.12Chr1227,494,34727,501,998
nsv5261840RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1227,647,28027,654,931

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16762205copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16762205Submitted genomicGRCh38.p13NC_000012.12Chr1227,494,34727,501,998
nssv16762205RemappedPerfectGRCh37.p13First PassNC_000012.11Chr1227,647,28027,654,931

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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