U.S. flag

An official website of the United States government

nsv6584518

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:944

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 93 SVs from 27 studies. See in: genome view    
    Submitted genomic120,039,507-120,040,450Question Mark
    Overlapping variant regions from other studies: 93 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):120,477,311-120,478,254Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6584518Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12120,039,507120,040,450
    nsv6584518RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12120,477,311120,478,254

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18224078inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18224078Submitted genomicNC_000012.12:g.120
    039507_120040450in
    v
    GRCh38 (hg38)NC_000012.12Chr12120,039,507120,040,450
    nssv18224078RemappedPerfectNC_000012.11:g.120
    477311_120478254in
    v
    GRCh37.p13First PassNC_000012.11Chr12120,477,311120,478,254

    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)
    nssv18224078<0.001834300
    Support Center