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nsv5547965

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 29 studies. See in: genome view    
Submitted genomic12,914,593-12,914,596Question Mark
Overlapping variant regions from other studies: 131 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):13,067,527-13,067,530Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5547965Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1212,914,59312,914,596
nsv5547965RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1213,067,52713,067,530

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053240insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053240Submitted genomicNC_000012.12:g.129
14593_12914596ins8
6
GRCh38 (hg38)NC_000012.12Chr1212,914,59312,914,596
nssv17053240RemappedPerfectNC_000012.11:g.130
67527_13067530ins8
6
GRCh37.p13First PassNC_000012.11Chr1213,067,52713,067,530

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)
nssv17053240<0.00146404
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