U.S. flag

An official website of the United States government

nsv6729519

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 162 SVs from 43 studies. See in: genome view    
    Submitted genomic44,022,301-44,067,000Question Mark
    Overlapping variant regions from other studies: 162 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):44,024,318-44,069,017Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6729519Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr444,022,30144,067,000
    nsv6729519RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr444,024,31844,069,017

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18495400deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18495400Submitted genomicNC_000004.12:g.440
    22301_44067000del
    GRCh38 (hg38)NC_000004.12Chr444,022,30144,067,000
    nssv18495400RemappedPerfectNC_000004.11:g.440
    24318_44069017del
    GRCh37.p13First PassNC_000004.11Chr444,024,31844,069,017

    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)
    nssv18495400<0.001113245460
    Support Center