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nsv6510440

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 309 SVs from 48 studies. See in: genome view    
    Submitted genomic36,497,701-36,503,700Question Mark
    Overlapping variant regions from other studies: 78 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):382,451-388,450Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6510440Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1736,497,70136,503,700
    nsv6510440RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003315949.1Chr17|NW_0
    03315949.1
    382,451388,450

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18180509duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18180509Submitted genomicNC_000017.11:g.364
    97701_36503700dup
    GRCh38 (hg38)NC_000017.11Chr1736,497,70136,503,700
    nssv18180509RemappedPerfectNW_003315949.1:g.3
    82451_388450dup
    GRCh37.p13First PassNW_003315949.1Chr17|NW_0
    03315949.1
    382,451388,450

    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)
    nssv18180509<0.001439144
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