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nsv6614592

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:476

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 98 SVs from 24 studies. See in: genome view    
    Submitted genomic35,079,113-35,079,588Question Mark
    Overlapping variant regions from other studies: 98 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):35,118,725-35,119,200Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6614592Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr735,079,11335,079,588
    nsv6614592RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr735,118,72535,119,200

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18228674duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18228674Submitted genomicNC_000007.14:g.350
    79113_35079588dup
    GRCh38 (hg38)NC_000007.14Chr735,079,11335,079,588
    nssv18228674RemappedPerfectNC_000007.13:g.351
    18725_35119200dup
    GRCh37.p13First PassNC_000007.13Chr735,118,72535,119,200

    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)
    nssv182286740.0015137828
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