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nsv4259477

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 18 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):56,897,651-56,897,709Question Mark
Overlapping variant regions from other studies: 17 SVs from 4 studies. See in: genome view    
Submitted genomic54,975,012-54,975,070Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4259477RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1756,897,65156,897,709
nsv4259477Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1754,975,01254,975,070

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15836552deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15836552RemappedPerfectNC_000017.11:g.568
97651_56897709del
GRCh38.p12First PassNC_000017.11Chr1756,897,65156,897,709
nssv15836552Submitted genomicNC_000017.10:g.549
75012_54975070del
GRCh37.p13NC_000017.10Chr1754,975,01254,975,070

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)
nssv158365524.6e-005121694
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