U.S. flag

An official website of the United States government

nsv6484504

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 23 studies. See in: genome view    
    Submitted genomic133,054,701-133,055,400Question Mark
    Overlapping variant regions from other studies: 109 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):133,631,287-133,631,986Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6484504Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12133,054,701133,055,400
    nsv6484504RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12133,631,287133,631,986

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17999221deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17999221Submitted genomicNC_000012.12:g.133
    054701_133055400de
    l
    GRCh38 (hg38)NC_000012.12Chr12133,054,701133,055,400
    nssv17999221RemappedPerfectNC_000012.11:g.133
    631287_133631986de
    l
    GRCh37.p13First PassNC_000012.11Chr12133,631,287133,631,986

    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)
    nssv17999221<0.0011838404
    Support Center