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nsv6453780

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 493 SVs from 67 studies. See in: genome view    
    Submitted genomic133,612,601-133,634,500Question Mark
    Overlapping variant regions from other studies: 493 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):135,426,105-135,448,004Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6453780Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10133,612,601133,634,500
    nsv6453780RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10135,426,105135,448,004

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18193864duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18193864Submitted genomicNC_000010.11:g.133
    612601_133634500du
    p
    GRCh38 (hg38)NC_000010.11Chr10133,612,601133,634,500
    nssv18193864RemappedPerfectNC_000010.10:g.135
    426105_135448004du
    p
    GRCh37.p13First PassNC_000010.10Chr10135,426,105135,448,004

    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)
    nssv181938640.00830239028
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