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nsv5529849

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:280

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 560 SVs from 53 studies. See in: genome view    
Submitted genomic15,049,745-15,050,024Question Mark
Overlapping variant regions from other studies: 560 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):15,143,602-15,143,881Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5529849Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1615,049,74515,050,024
nsv5529849RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1615,143,60215,143,881

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706494deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706494Submitted genomicNC_000016.10:g.150
49745_15050024del
GRCh38 (hg38)NC_000016.10Chr1615,049,74515,050,024
nssv17706494RemappedPerfectNC_000016.9:g.1514
3602_15143881del
GRCh37.p13First PassNC_000016.9Chr1615,143,60215,143,881

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)
nssv17706494<0.00116404
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