U.S. flag

An official website of the United States government

nsv6544628

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:421

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 20 studies. See in: genome view    
    Submitted genomic179,633,665-179,634,085Question Mark
    Overlapping variant regions from other studies: 155 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):179,602,800-179,603,220Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6544628Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1179,633,665179,634,085
    nsv6544628RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1179,602,800179,603,220

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18248831inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18248831Submitted genomicNC_000001.11:g.179
    633665_179634085in
    v
    GRCh38 (hg38)NC_000001.11Chr1179,633,665179,634,085
    nssv18248831RemappedPerfectNC_000001.10:g.179
    602800_179603220in
    v
    GRCh37.p13First PassNC_000001.10Chr1179,602,800179,603,220

    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)
    nssv18248831<0.001135570
    Support Center