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nsv7087753

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,296

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 302 SVs from 28 studies. See in: genome view    
    Submitted genomic46,456,236-46,477,531Question Mark
    Overlapping variant regions from other studies: 302 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):46,315,671-46,336,966Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7087753Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX46,456,23646,477,531
    nsv7087753RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX46,315,67146,336,966

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18656901duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18656901Submitted genomicNC_000023.11:g.464
    56236_46477531dup
    GRCh38 (hg38)NC_000023.11ChrX46,456,23646,477,531
    nssv18656901RemappedPerfectNC_000023.10:g.463
    15671_46336966dup
    GRCh37.p13First PassNC_000023.10ChrX46,315,67146,336,966

    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)
    nssv18656901<0.00144216749
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