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nsv5563034

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 14 studies. See in: genome view    
Submitted genomic47,820,538-47,820,543Question Mark
Overlapping variant regions from other studies: 141 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):45,897,904-45,897,909Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563034Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1747,820,53847,820,543
nsv5563034RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1745,897,90445,897,909

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713517sequence alterationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17713517Submitted genomicGRCh38 (hg38)NC_000017.11Chr1747,820,53847,820,543
nssv17713517RemappedPerfectGRCh37.p13First PassNC_000017.10Chr1745,897,90445,897,909

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)
nssv17713517<0.00116404
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