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nsv7065486

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:172,579

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 611 SVs from 63 studies. See in: genome view    
    Submitted genomic65,309,443-65,482,021Question Mark
    Overlapping variant regions from other studies: 611 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):65,076,914-65,249,492Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065486Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1165,309,44365,482,021
    nsv7065486RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1165,076,91465,249,492

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731052inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731052Submitted genomicNC_000011.10:g.653
    09443_65482021inv
    GRCh38 (hg38)NC_000011.10Chr1165,309,44365,482,021
    nssv18731052RemappedPerfectNC_000011.9:g.6507
    6914_65249492inv
    GRCh37.p13First PassNC_000011.9Chr1165,076,91465,249,492

    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)
    nssv187310524e-061276268
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