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nsv6722937

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,320,437

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2753 SVs from 94 studies. See in: genome view    
    Submitted genomic136,813,721-138,134,157Question Mark
    Overlapping variant regions from other studies: 2753 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):136,532,563-137,852,999Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6722937Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3136,813,721138,134,157
    nsv6722937RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3136,532,563137,852,999

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18473605deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18473605Submitted genomicNC_000003.12:g.136
    813721_138134157de
    l
    GRCh38 (hg38)NC_000003.12Chr3136,813,721138,134,157
    nssv18473605RemappedPerfectNC_000003.11:g.136
    532563_137852999de
    l
    GRCh37.p13First PassNC_000003.11Chr3136,532,563137,852,999

    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)
    nssv184736052.8e-058276106
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