U.S. flag

An official website of the United States government

nsv7048311

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,781

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 17 studies. See in: genome view    
    Submitted genomic136,780,676-136,782,456Question Mark
    Overlapping variant regions from other studies: 103 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):137,101,814-137,103,594Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048311Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6136,780,676136,782,456
    nsv7048311RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6137,101,814137,103,594

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18779588inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18779588Submitted genomicNC_000006.12:g.136
    780676_136782456in
    v
    GRCh38 (hg38)NC_000006.12Chr6136,780,676136,782,456
    nssv18779588RemappedPerfectNC_000006.11:g.137
    101814_137103594in
    v
    GRCh37.p13First PassNC_000006.11Chr6137,101,814137,103,594

    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)
    nssv187795884e-061276268
    Support Center