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nsv7059778

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,223

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 31 studies. See in: genome view    
    Submitted genomic65,293,487-65,314,709Question Mark
    Overlapping variant regions from other studies: 132 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):65,327,390-65,348,612Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059778Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1665,293,48765,314,709
    nsv7059778RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1665,327,39065,348,612

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758140inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758140Submitted genomicNC_000016.10:g.652
    93487_65314709inv
    GRCh38 (hg38)NC_000016.10Chr1665,293,48765,314,709
    nssv18758140RemappedPerfectNC_000016.9:g.6532
    7390_65348612inv
    GRCh37.p13First PassNC_000016.9Chr1665,327,39065,348,612

    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)
    nssv187581407e-062276260
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