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nsv5457616

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,629

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 24 studies. See in: genome view    
Submitted genomic132,734,103-132,740,731Question Mark
Overlapping variant regions from other studies: 115 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):133,055,242-133,061,870Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5457616Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6132,734,103132,740,731
nsv5457616RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6133,055,242133,061,870

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16970085deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16970085Submitted genomicNC_000006.12:g.132
734103_132740731de
l
GRCh38 (hg38)NC_000006.12Chr6132,734,103132,740,731
nssv16970085RemappedPerfectNC_000006.11:g.133
055242_133061870de
l
GRCh37.p13First PassNC_000006.11Chr6133,055,242133,061,870

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)
nssv169700850.00176404
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