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nsv6751894

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,352

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 34 studies. See in: genome view    
    Submitted genomic79,045,900-79,054,251Question Mark
    Overlapping variant regions from other studies: 137 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):79,967,054-79,975,405Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6751894Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr479,045,90079,054,251
    nsv6751894RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr479,967,05479,975,405

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18502155deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18502155Submitted genomicNC_000004.12:g.790
    45900_79054251del
    GRCh38 (hg38)NC_000004.12Chr479,045,90079,054,251
    nssv18502155RemappedPerfectNC_000004.11:g.799
    67054_79975405del
    GRCh37.p13First PassNC_000004.11Chr479,967,05479,975,405

    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)
    nssv185021554e-061276210
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