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nsv4528628

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:531,396

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 441 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):68,538,683-69,070,078Question Mark
Overlapping variant regions from other studies: 441 SVs from 19 studies. See in: genome view    
Submitted genomic68,306,151-68,837,546Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4528628RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1168,538,68369,070,078
nsv4528628Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1168,306,15168,837,546

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15947443duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15947443RemappedPerfectNC_000011.10:g.685
38683_69070078dup
GRCh38.p12First PassNC_000011.10Chr1168,538,68369,070,078
nssv15947443Submitted genomicNC_000011.9:g.6830
6151_68837546dup
GRCh37.p13NC_000011.9Chr1168,306,15168,837,546

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)
nssv159474434.6e-005121694
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