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nsv6513563

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,055

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 34 studies. See in: genome view    
    Submitted genomic32,399,553-32,432,607Question Mark
    Overlapping variant regions from other studies: 193 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):30,726,572-30,759,626Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6513563Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1732,399,55332,432,607
    nsv6513563RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1730,726,57230,759,626

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18191306duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18191306Submitted genomicNC_000017.11:g.323
    99553_32432607dup
    GRCh38 (hg38)NC_000017.11Chr1732,399,55332,432,607
    nssv18191306RemappedPerfectNC_000017.10:g.307
    26572_30759626dup
    GRCh37.p13First PassNC_000017.10Chr1730,726,57230,759,626

    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)
    nssv18191306<0.001739280
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