U.S. flag

An official website of the United States government

nsv6332313

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:426

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 20 studies. See in: genome view    
    Submitted genomic193,085,970-193,086,395Question Mark
    Overlapping variant regions from other studies: 139 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):193,055,100-193,055,525Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6332313Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1193,085,970193,086,395
    nsv6332313RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1193,055,100193,055,525

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18055558deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18055558Submitted genomicNC_000001.11:g.193
    085970_193086395de
    l
    GRCh38 (hg38)NC_000001.11Chr1193,085,970193,086,395
    nssv18055558RemappedPerfectNC_000001.10:g.193
    055100_193055525de
    l
    GRCh37.p13First PassNC_000001.10Chr1193,055,100193,055,525

    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)
    nssv18055558<0.0012538128
    Support Center