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nsv5471051

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:189

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 82 SVs from 17 studies. See in: genome view    
Submitted genomic132,338,042-132,338,230Question Mark
Overlapping variant regions from other studies: 82 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):132,659,181-132,659,369Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5471051Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6132,338,042132,338,230
nsv5471051RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6132,659,181132,659,369

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16970057deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16970057Submitted genomicNC_000006.12:g.132
338042_132338230de
l
GRCh38 (hg38)NC_000006.12Chr6132,338,042132,338,230
nssv16970057RemappedPerfectNC_000006.11:g.132
659181_132659369de
l
GRCh37.p13First PassNC_000006.11Chr6132,659,181132,659,369

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)
nssv16970057<0.00136404
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