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nsv5466428

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 81 SVs from 18 studies. See in: genome view    
Submitted genomic132,314,608-132,314,686Question Mark
Overlapping variant regions from other studies: 81 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):132,635,747-132,635,825Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5466428Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6132,314,608132,314,686
nsv5466428RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6132,635,747132,635,825

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16970056deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16970056Submitted genomicNC_000006.12:g.132
314608_132314686de
l
GRCh38 (hg38)NC_000006.12Chr6132,314,608132,314,686
nssv16970056RemappedPerfectNC_000006.11:g.132
635747_132635825de
l
GRCh37.p13First PassNC_000006.11Chr6132,635,747132,635,825

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)
nssv16970056<0.00126404
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