U.S. flag

An official website of the United States government

nsv6847027

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,871

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 161 SVs from 19 studies. See in: genome view    
    Submitted genomic102,802,032-102,805,902Question Mark
    Overlapping variant regions from other studies: 161 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):103,814,260-103,818,130Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6847027Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8102,802,032102,805,902
    nsv6847027RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8103,814,260103,818,130

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18549380deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18549380Submitted genomicNC_000008.11:g.102
    802032_102805902de
    l
    GRCh38 (hg38)NC_000008.11Chr8102,802,032102,805,902
    nssv18549380RemappedPerfectNC_000008.10:g.103
    814260_103818130de
    l
    GRCh37.p13First PassNC_000008.10Chr8103,814,260103,818,130

    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)
    nssv185493804e-061276140
    Support Center