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nsv6668387

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:139,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 459 SVs from 62 studies. See in: genome view    
    Submitted genomic43,658,901-43,798,200Question Mark
    Overlapping variant regions from other studies: 459 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):43,886,040-44,025,339Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6668387Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr243,658,90143,798,200
    nsv6668387RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr243,886,04044,025,339

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18664624duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18664624Submitted genomicNC_000002.12:g.436
    58901_43798200dup
    GRCh38 (hg38)NC_000002.12Chr243,658,90143,798,200
    nssv18664624RemappedPerfectNC_000002.11:g.438
    86040_44025339dup
    GRCh37.p13First PassNC_000002.11Chr243,886,04044,025,339

    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)
    nssv186646244e-061275460
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