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nsv5516522

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 161 SVs from 26 studies. See in: genome view    
Submitted genomic74,903,583-74,903,639Question Mark
Overlapping variant regions from other studies: 161 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):75,195,924-75,195,980Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5516522Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1574,903,58374,903,639
nsv5516522RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1575,195,92475,195,980

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702034deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702034Submitted genomicNC_000015.10:g.749
03583_74903639del
GRCh38 (hg38)NC_000015.10Chr1574,903,58374,903,639
nssv17702034RemappedPerfectNC_000015.9:g.7519
5924_75195980del
GRCh37.p13First PassNC_000015.9Chr1575,195,92475,195,980

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)
nssv17702034<0.00136404
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