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nsv7072074

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,169,865

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3098 SVs from 98 studies. See in: genome view    
    Submitted genomic10,322,193-11,492,057Question Mark
    Overlapping variant regions from other studies: 3098 SVs from 98 studies. See in: genome view    
    Remapped(Score: Perfect):10,225,510-11,395,374Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072074Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1710,322,19311,492,057
    nsv7072074RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1710,225,51011,395,374

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758920inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758920Submitted genomicNC_000017.11:g.103
    22193_11492057inv
    GRCh38 (hg38)NC_000017.11Chr1710,322,19311,492,057
    nssv18758920RemappedPerfectNC_000017.10:g.102
    25510_11395374inv
    GRCh37.p13First PassNC_000017.10Chr1710,225,51011,395,374

    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)
    nssv187589204e-061276266
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