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nsv6534117

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:389

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 28 studies. See in: genome view    
    Submitted genomic49,455,072-49,455,460Question Mark
    Overlapping variant regions from other studies: 90 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):49,958,329-49,958,717Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6534117Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1949,455,07249,455,460
    nsv6534117RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,958,32949,958,717

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18198248duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18198248Submitted genomicNC_000019.10:g.494
    55072_49455460dup
    GRCh38 (hg38)NC_000019.10Chr1949,455,07249,455,460
    nssv18198248RemappedPerfectNC_000019.9:g.4995
    8329_49958717dup
    GRCh37.p13First PassNC_000019.9Chr1949,958,32949,958,717

    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)
    nssv18198248<0.0011236490
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