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nsv6744597

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,143

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 30 studies. See in: genome view    
    Submitted genomic75,528,446-75,532,588Question Mark
    Overlapping variant regions from other studies: 121 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):76,453,656-76,457,798Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6744597Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr475,528,44675,532,588
    nsv6744597RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr476,453,65676,457,798

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18500428deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18500428Submitted genomicNC_000004.12:g.755
    28446_75532588del
    GRCh38 (hg38)NC_000004.12Chr475,528,44675,532,588
    nssv18500428RemappedPerfectNC_000004.11:g.764
    53656_76457798del
    GRCh37.p13First PassNC_000004.11Chr476,453,65676,457,798

    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)
    nssv185004284e-061276100
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