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nsv5526736

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 24 studies. See in: genome view    
Submitted genomic42,235,980-42,241,980Question Mark
Overlapping variant regions from other studies: 141 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):40,387,998-40,393,998Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5526736Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1742,235,98042,241,980
nsv5526736RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1740,387,99840,393,998

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713234deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713234Submitted genomicNC_000017.11:g.422
35980_42241980del
GRCh38 (hg38)NC_000017.11Chr1742,235,98042,241,980
nssv17713234RemappedPerfectNC_000017.10:g.403
87998_40393998del
GRCh37.p13First PassNC_000017.10Chr1740,387,99840,393,998

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)
nssv17713234<0.00116398
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