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nsv7047961

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,105,583

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 17732 SVs from 123 studies. See in: genome view    
    Submitted genomic123,155,784-130,261,366Question Mark
    Overlapping variant regions from other studies: 17738 SVs from 123 studies. See in: genome view    
    Remapped(Score: Good):122,795,838-129,901,206Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047961Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7123,155,784130,261,366
    nsv7047961RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7122,795,838129,901,206

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778915inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778915Submitted genomicNC_000007.14:g.123
    155784_130261366in
    v
    GRCh38 (hg38)NC_000007.14Chr7123,155,784130,261,366
    nssv18778915RemappedGoodNC_000007.13:g.122
    795838_129901206in
    v
    GRCh37.p13First PassNC_000007.13Chr7122,795,838129,901,206

    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)
    nssv187789154e-060276268
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