U.S. flag

An official website of the United States government

nsv6344905

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:148,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 483 SVs from 51 studies. See in: genome view    
    Submitted genomic185,163,501-185,312,400Question Mark
    Overlapping variant regions from other studies: 483 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):186,028,228-186,177,127Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6344905Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2185,163,501185,312,400
    nsv6344905RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2186,028,228186,177,127

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18082498deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18082498Submitted genomicNC_000002.12:g.185
    163501_185312400de
    l
    GRCh38 (hg38)NC_000002.12Chr2185,163,501185,312,400
    nssv18082498RemappedPerfectNC_000002.11:g.186
    028228_186177127de
    l
    GRCh37.p13First PassNC_000002.11Chr2186,028,228186,177,127

    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)
    nssv18082498<0.001238732
    Support Center