U.S. flag

An official website of the United States government

nsv7075067

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:122

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 211 SVs from 42 studies. See in: genome view    
    Submitted genomic27,595,117-27,595,238Question Mark
    Overlapping variant regions from other studies: 211 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):27,748,050-27,748,171Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075067Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1227,595,11727,595,238
    nsv7075067RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1227,748,05027,748,171

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18751737inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18751737Submitted genomicNC_000012.12:g.275
    95117_27595238inv
    GRCh38 (hg38)NC_000012.12Chr1227,595,11727,595,238
    nssv18751737RemappedPerfectNC_000012.11:g.277
    48050_27748171inv
    GRCh37.p13First PassNC_000012.11Chr1227,748,05027,748,171

    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)
    nssv187517374e-061276268
    Support Center