U.S. flag

An official website of the United States government

nsv6677161

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
    Submitted genomic231,375,311-231,375,343Question Mark
    Overlapping variant regions from other studies: 131 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):231,511,057-231,511,089Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6677161Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1231,375,311231,375,343
    nsv6677161RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1231,511,057231,511,089

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18368533deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18368533Submitted genomicNC_000001.11:g.231
    375311_231375343de
    l
    GRCh38 (hg38)NC_000001.11Chr1231,375,311231,375,343
    nssv18368533RemappedPerfectNC_000001.10:g.231
    511057_231511089de
    l
    GRCh37.p13First PassNC_000001.10Chr1231,511,057231,511,089

    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)
    nssv183685330.517109490209816
    Support Center