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nsv6496568

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,482

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 49 studies. See in: genome view    
    Submitted genomic94,362,247-94,370,728Question Mark
    Overlapping variant regions from other studies: 141 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):94,828,584-94,837,065Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6496568Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1494,362,24794,370,728
    nsv6496568RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1494,828,58494,837,065

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18193048duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18193048Submitted genomicNC_000014.9:g.9436
    2247_94370728dup
    GRCh38 (hg38)NC_000014.9Chr1494,362,24794,370,728
    nssv18193048RemappedPerfectNC_000014.8:g.9482
    8584_94837065dup
    GRCh37.p13First PassNC_000014.8Chr1494,828,58494,837,065

    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)
    nssv18193048<0.001128702
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