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nsv6894589

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:557,376

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1708 SVs from 84 studies. See in: genome view    
    Submitted genomic64,506,570-65,063,945Question Mark
    Overlapping variant regions from other studies: 1708 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):66,266,327-66,823,703Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6894589Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1064,506,57065,063,945
    nsv6894589RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1066,266,32766,823,703

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586331duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586331Submitted genomicNC_000010.11:g.645
    06570_65063945dup
    GRCh38 (hg38)NC_000010.11Chr1064,506,57065,063,945
    nssv18586331RemappedPerfectNC_000010.10:g.662
    66327_66823703dup
    GRCh37.p13First PassNC_000010.10Chr1066,266,32766,823,703

    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)
    nssv185863314e-061272266
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