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nsv7060144

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,065

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 370 SVs from 25 studies. See in: genome view    
    Submitted genomic3,662,848-3,666,912Question Mark
    Overlapping variant regions from other studies: 371 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):3,580,889-3,584,953Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060144Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX3,662,8483,666,912
    nsv7060144RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX3,580,8893,584,953

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18455585deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18455585Submitted genomicNC_000023.11:g.366
    2848_3666912del
    GRCh38 (hg38)NC_000023.11ChrX3,662,8483,666,912
    nssv18455585RemappedPerfectNC_000023.10:g.358
    0889_3584953del
    GRCh37.p13First PassNC_000023.10ChrX3,580,8893,584,953

    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)
    nssv18455585<0.00174216374
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