U.S. flag

An official website of the United States government

nsv7047602

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,767

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 970 SVs from 69 studies. See in: genome view    
    Submitted genomic242,052,489-242,058,255Question Mark
    Overlapping variant regions from other studies: 970 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):242,994,640-243,000,406Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047602Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2242,052,489242,058,255
    nsv7047602RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2242,994,640243,000,406

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769117inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769117Submitted genomicNC_000002.12:g.242
    052489_242058255in
    v
    GRCh38 (hg38)NC_000002.12Chr2242,052,489242,058,255
    nssv18769117RemappedPerfectNC_000002.11:g.242
    994640_243000406in
    v
    GRCh37.p13First PassNC_000002.11Chr2242,994,640243,000,406

    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)
    nssv187691174e-061276268
    Support Center