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nsv4578224

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 61 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):14,374,988-14,374,988Question Mark
Overlapping variant regions from other studies: 62 SVs from 10 studies. See in: genome view    
Submitted genomic14,527,922-14,527,922Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578224RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1214,374,98814,374,988
nsv4578224Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1214,527,92214,527,922

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15997896sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15997896RemappedPerfectNC_000012.12:g.143
74988_14374989ins7
74
GRCh38.p12First PassNC_000012.12Chr1214,374,98814,374,988
nssv15997896Submitted genomicNC_000012.11:g.145
27922_14527923ins7
74
GRCh37.p13NC_000012.11Chr1214,527,92214,527,922

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)
nssv15997896<0.001421694
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