U.S. flag

An official website of the United States government

nsv6414263

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:671

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 27 studies. See in: genome view    
    Submitted genomic42,995,198-42,995,868Question Mark
    Overlapping variant regions from other studies: 105 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):42,962,936-42,963,606Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6414263Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr642,995,19842,995,868
    nsv6414263RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr642,962,93642,963,606

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18236070duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18236070Submitted genomicNC_000006.12:g.429
    95198_42995868dup
    GRCh38 (hg38)NC_000006.12Chr642,995,19842,995,868
    nssv18236070RemappedPerfectNC_000006.11:g.429
    62936_42963606dup
    GRCh37.p13First PassNC_000006.11Chr642,962,93642,963,606

    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)
    nssv18236070<0.001137546
    Support Center