U.S. flag

An official website of the United States government

nsv6473551

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:23,130

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 324 SVs from 58 studies. See in: genome view    
    Submitted genomic7,770,716-7,793,845Question Mark
    Overlapping variant regions from other studies: 324 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):7,923,312-7,946,441Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6473551Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr127,770,7167,793,845
    nsv6473551RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr127,923,3127,946,441

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18188839duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18188839Submitted genomicNC_000012.12:g.777
    0716_7793845dup
    GRCh38 (hg38)NC_000012.12Chr127,770,7167,793,845
    nssv18188839RemappedPerfectNC_000012.11:g.792
    3312_7946441dup
    GRCh37.p13First PassNC_000012.11Chr127,923,3127,946,441

    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)
    nssv18188839<0.001139272
    Support Center