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nsv5255604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,580

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 568 SVs from 70 studies. See in: genome view    
Submitted genomic133,611,182-133,632,761Question Mark
Overlapping variant regions from other studies: 567 SVs from 70 studies. See in: genome view    
Remapped(Score: Perfect):135,424,686-135,446,265Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5255604Submitted genomicGRCh38.p13Primary AssemblyNC_000010.11Chr10133,611,182133,632,761
nsv5255604RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10135,424,686135,446,265

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16762298copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16762298Submitted genomicGRCh38.p13NC_000010.11Chr10133,611,182133,632,761
nssv16762298RemappedPerfectGRCh37.p13First PassNC_000010.10Chr10135,424,686135,446,265

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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