U.S. flag

An official website of the United States government

nsv6754965

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,060

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 31 studies. See in: genome view    
    Submitted genomic71,405,920-71,410,979Question Mark
    Overlapping variant regions from other studies: 127 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):72,271,637-72,276,696Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6754965Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr471,405,92071,410,979
    nsv6754965RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr472,271,63772,276,696

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18499471deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18499471Submitted genomicNC_000004.12:g.714
    05920_71410979del
    GRCh38 (hg38)NC_000004.12Chr471,405,92071,410,979
    nssv18499471RemappedPerfectNC_000004.11:g.722
    71637_72276696del
    GRCh37.p13First PassNC_000004.11Chr472,271,63772,276,696

    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)
    nssv184994714e-061275960
    Support Center