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nsv6995921

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,606

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 180 SVs from 50 studies. See in: genome view    
    Submitted genomic7,433,470-7,438,075Question Mark
    Overlapping variant regions from other studies: 180 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):7,336,789-7,341,394Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995921Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr177,433,4707,438,075
    nsv6995921RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr177,336,7897,341,394

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18414215deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18414215Submitted genomicNC_000017.11:g.743
    3470_7438075del
    GRCh38 (hg38)NC_000017.11Chr177,433,4707,438,075
    nssv18414215RemappedPerfectNC_000017.10:g.733
    6789_7341394del
    GRCh37.p13First PassNC_000017.10Chr177,336,7897,341,394

    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)
    nssv184142157e-062276206
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