U.S. flag

An official website of the United States government

nsv7060606

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58,526

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 536 SVs from 52 studies. See in: genome view    
    Submitted genomic3,680,314-3,738,839Question Mark
    Overlapping variant regions from other studies: 537 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):3,598,355-3,656,880Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060606Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX3,680,3143,738,839
    nsv7060606RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX3,598,3553,656,880

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18658320duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18658320Submitted genomicNC_000023.11:g.368
    0314_3738839dup
    GRCh38 (hg38)NC_000023.11ChrX3,680,3143,738,839
    nssv18658320RemappedPerfectNC_000023.10:g.359
    8355_3656880dup
    GRCh37.p13First PassNC_000023.10ChrX3,598,3553,656,880

    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)
    nssv186583201.4e-053214286
    Support Center