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nsv6846146

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:209

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 19 studies. See in: genome view    
    Submitted genomic64,795,253-64,795,461Question Mark
    Overlapping variant regions from other studies: 116 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):65,707,810-65,708,018Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6846146Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr864,795,25364,795,461
    nsv6846146RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr865,707,81065,708,018

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732447duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732447Submitted genomicNC_000008.11:g.647
    95253_64795461dup
    GRCh38 (hg38)NC_000008.11Chr864,795,25364,795,461
    nssv18732447RemappedPerfectNC_000008.10:g.657
    07810_65708018dup
    GRCh37.p13First PassNC_000008.10Chr865,707,81065,708,018

    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)
    nssv187324474e-061237938
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