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nsv5432641

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 135 SVs from 28 studies. See in: genome view    
Submitted genomic12,533,767-12,533,818Question Mark
Overlapping variant regions from other studies: 136 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):12,686,701-12,686,752Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5432641Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1212,533,76712,533,818
nsv5432641RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1212,686,70112,686,752

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053187alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053187Submitted genomicNC_000012.12:g.125
33767_12533818ins2
68
GRCh38 (hg38)NC_000012.12Chr1212,533,76712,533,818
nssv17053187RemappedPerfectNC_000012.11:g.126
86701_12686752ins2
68
GRCh37.p13First PassNC_000012.11Chr1212,686,70112,686,752

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)
nssv17053187<0.00146404
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