U.S. flag

An official website of the United States government

nsv6609550

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 98 SVs from 27 studies. See in: genome view    
    Submitted genomic150,385,601-150,386,800Question Mark
    Overlapping variant regions from other studies: 98 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):150,706,737-150,707,936Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6609550Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6150,385,601150,386,800
    nsv6609550RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6150,706,737150,707,936

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18141025deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18141025Submitted genomicNC_000006.12:g.150
    385601_150386800de
    l
    GRCh38 (hg38)NC_000006.12Chr6150,385,601150,386,800
    nssv18141025RemappedPerfectNC_000006.11:g.150
    706737_150707936de
    l
    GRCh37.p13First PassNC_000006.11Chr6150,706,737150,707,936

    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)
    nssv18141025<0.001238900
    Support Center