nsv6877500

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,870

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 32 studies. See in: genome view    
    Submitted genomic110,195,461-110,206,330Question Mark
    Overlapping variant regions from other studies: 131 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):112,957,741-112,968,610Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6877500Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9110,195,461110,206,330
    nsv6877500RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9112,957,741112,968,610

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18563027deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18563027Submitted genomicNC_000009.12:g.110
    195461_110206330de
    l
    GRCh38 (hg38)NC_000009.12Chr9110,195,461110,206,330
    nssv18563027RemappedPerfectNC_000009.11:g.112
    957741_112968610de
    l
    GRCh37.p13First PassNC_000009.11Chr9112,957,741112,968,610

    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)
    nssv185630275.7e-0516275794
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