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nsv6834556

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,039

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 179 SVs from 46 studies. See in: genome view    
    Submitted genomic75,059,872-75,062,910Question Mark
    Overlapping variant regions from other studies: 47 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):2,589,108-2,592,146Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6834556Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr775,059,87275,062,910
    nsv6834556RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003871064.1Chr7|NW_00
    3871064.1
    2,589,1082,592,146

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18544614deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18544614Submitted genomicNC_000007.14:g.750
    59872_75062910del
    GRCh38 (hg38)NC_000007.14Chr775,059,87275,062,910
    nssv18544614RemappedPerfectNW_003871064.1:g.2
    589108_2592146del
    GRCh37.p13First PassNW_003871064.1Chr7|NW_00
    3871064.1
    2,589,1082,592,146

    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)
    nssv185446144e-061276144
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