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nsv6651036

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:47,912

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 186 SVs from 42 studies. See in: genome view    
    Submitted genomic48,304,266-48,352,177Question Mark
    Overlapping variant regions from other studies: 186 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):48,769,938-48,817,849Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6651036Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr148,304,26648,352,177
    nsv6651036RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr148,769,93848,817,849

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18409465deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18409465Submitted genomicNC_000001.11:g.483
    04266_48352177del
    GRCh38 (hg38)NC_000001.11Chr148,304,26648,352,177
    nssv18409465RemappedPerfectNC_000001.10:g.487
    69938_48817849del
    GRCh37.p13First PassNC_000001.10Chr148,769,93848,817,849

    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)
    nssv184094654e-061276118
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