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nsv6737484

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51,137

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 217 SVs from 32 studies. See in: genome view    
    Submitted genomic17,971,732-18,022,868Question Mark
    Overlapping variant regions from other studies: 217 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):17,973,355-18,024,491Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6737484Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr417,971,73218,022,868
    nsv6737484RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr417,973,35518,024,491

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18688364duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18688364Submitted genomicNC_000004.12:g.179
    71732_18022868dup
    GRCh38 (hg38)NC_000004.12Chr417,971,73218,022,868
    nssv18688364RemappedPerfectNC_000004.11:g.179
    73355_18024491dup
    GRCh37.p13First PassNC_000004.11Chr417,973,35518,024,491

    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)
    nssv186883644e-061275220
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