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nsv6528212

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:696

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 229 SVs from 38 studies. See in: genome view    
    Submitted genomic82,318,653-82,319,348Question Mark
    Overlapping variant regions from other studies: 229 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):80,276,529-80,277,224Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6528212Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1782,318,65382,319,348
    nsv6528212RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1780,276,52980,277,224

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18038278deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18038278Submitted genomicNC_000017.11:g.823
    18653_82319348del
    GRCh38 (hg38)NC_000017.11Chr1782,318,65382,319,348
    nssv18038278RemappedPerfectNC_000017.10:g.802
    76529_80277224del
    GRCh37.p13First PassNC_000017.10Chr1780,276,52980,277,224

    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)
    nssv180382780.00715923674
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