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nsv7072039

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,634,049

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7948 SVs from 116 studies. See in: genome view    
    Submitted genomic79,903,600-82,537,648Question Mark
    Overlapping variant regions from other studies: 7944 SVs from 116 studies. See in: genome view    
    Remapped(Score: Good):79,937,497-82,571,253Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072039Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1679,903,60082,537,648
    nsv7072039RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1679,937,49782,571,253

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756569inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756569Submitted genomicNC_000016.10:g.799
    03600_82537648inv
    GRCh38 (hg38)NC_000016.10Chr1679,903,60082,537,648
    nssv18756569RemappedGoodNC_000016.9:g.7993
    7497_82571253inv
    GRCh37.p13First PassNC_000016.9Chr1679,937,49782,571,253

    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)
    nssv187565697e-062274544
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