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nsv6919314

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,088

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 40 studies. See in: genome view    
    Submitted genomic24,710,140-24,722,227Question Mark
    Overlapping variant regions from other studies: 193 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):25,284,278-25,296,365Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6919314Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1324,710,14024,722,227
    nsv6919314RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1325,284,27825,296,365

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18603412duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18603412Submitted genomicNC_000013.11:g.247
    10140_24722227dup
    GRCh38 (hg38)NC_000013.11Chr1324,710,14024,722,227
    nssv18603412RemappedPerfectNC_000013.10:g.252
    84278_25296365dup
    GRCh37.p13First PassNC_000013.10Chr1325,284,27825,296,365

    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)
    nssv186034122.8e-058275672
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