U.S. flag

An official website of the United States government

nsv6961202

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:96,084

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 345 SVs from 50 studies. See in: genome view    
    Submitted genomic67,495,999-67,592,082Question Mark
    Overlapping variant regions from other studies: 345 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):67,962,716-68,058,799Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6961202Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1467,495,99967,592,082
    nsv6961202RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1467,962,71668,058,799

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615337duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615337Submitted genomicNC_000014.9:g.6749
    5999_67592082dup
    GRCh38 (hg38)NC_000014.9Chr1467,495,99967,592,082
    nssv18615337RemappedPerfectNC_000014.8:g.6796
    2716_68058799dup
    GRCh37.p13First PassNC_000014.8Chr1467,962,71668,058,799

    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)
    nssv186153377e-062275890
    Support Center