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nsv6332732

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 21 studies. See in: genome view    
    Submitted genomic192,342,201-192,342,900Question Mark
    Overlapping variant regions from other studies: 143 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):192,311,331-192,312,030Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6332732Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1192,342,201192,342,900
    nsv6332732RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1192,311,331192,312,030

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18055481deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18055481Submitted genomicNC_000001.11:g.192
    342201_192342900de
    l
    GRCh38 (hg38)NC_000001.11Chr1192,342,201192,342,900
    nssv18055481RemappedPerfectNC_000001.10:g.192
    311331_192312030de
    l
    GRCh37.p13First PassNC_000001.10Chr1192,311,331192,312,030

    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)
    nssv18055481<0.001737708
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