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nsv5202671

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,700

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 159 SVs from 30 studies. See in: genome view    
Submitted genomic62,600,201-62,606,900Question Mark
Overlapping variant regions from other studies: 159 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):63,065,872-63,072,571Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5202671Submitted genomicGRCh38.p13Primary AssemblyNC_000001.11Chr162,600,20162,606,900
nsv5202671RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr163,065,87263,072,571

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16823464copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16823464Submitted genomicGRCh38.p13NC_000001.11Chr162,600,20162,606,900
nssv16823464RemappedPerfectGRCh37.p13First PassNC_000001.10Chr163,065,87263,072,571

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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