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nsv5530825

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,037

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 142 SVs from 29 studies. See in: genome view    
Submitted genomic64,814,251-64,818,287Question Mark
Overlapping variant regions from other studies: 142 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):62,810,369-62,814,405Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530825Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1764,814,25164,818,287
nsv5530825RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1762,810,36962,814,405

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714094deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714094Submitted genomicNC_000017.11:g.648
14251_64818287del
GRCh38 (hg38)NC_000017.11Chr1764,814,25164,818,287
nssv17714094RemappedPerfectNC_000017.10:g.628
10369_62814405del
GRCh37.p13First PassNC_000017.10Chr1762,810,36962,814,405

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv177140940.00196404
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