U.S. flag

An official website of the United States government

nsv7056877

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:442,447

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3036 SVs from 109 studies. See in: genome view    
    Submitted genomic16,489,319-16,931,765Question Mark
    Overlapping variant regions from other studies: 3041 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):16,815,814-17,258,260Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056877Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr116,489,31916,931,765
    nsv7056877RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr116,815,81417,258,260

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18733026inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18733026Submitted genomicNC_000001.11:g.164
    89319_16931765inv
    GRCh38 (hg38)NC_000001.11Chr116,489,31916,931,765
    nssv18733026RemappedPerfectNC_000001.10:g.168
    15814_17258260inv
    GRCh37.p13First PassNC_000001.10Chr116,815,81417,258,260

    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)
    nssv187330264e-061276268
    Support Center