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nsv6808085

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,076

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 19 studies. See in: genome view    
    Submitted genomic83,350,302-83,356,377Question Mark
    Overlapping variant regions from other studies: 108 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):84,060,021-84,066,096Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6808085Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr683,350,30283,356,377
    nsv6808085RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr684,060,02184,066,096

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18529091deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18529091Submitted genomicNC_000006.12:g.833
    50302_83356377del
    GRCh38 (hg38)NC_000006.12Chr683,350,30283,356,377
    nssv18529091RemappedPerfectNC_000006.11:g.840
    60021_84066096del
    GRCh37.p13First PassNC_000006.11Chr684,060,02184,066,096

    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)
    nssv185290914e-061276232
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