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nsv5523242

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 503 SVs from 66 studies. See in: genome view    
Submitted genomic36,474,874-36,560,874Question Mark
Overlapping variant regions from other studies: 503 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):36,965,776-37,051,776Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523242Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,474,87436,560,874
nsv5523242RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,965,77637,051,776

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723103deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723103Submitted genomicNC_000019.10:g.364
74874_36560874del
GRCh38 (hg38)NC_000019.10Chr1936,474,87436,560,874
nssv17723103RemappedPerfectNC_000019.9:g.3696
5776_37051776del
GRCh37.p13First PassNC_000019.9Chr1936,965,77637,051,776

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)
nssv17723103<0.00116402
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