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nsv7011400

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,501

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 27 studies. See in: genome view    
    Submitted genomic47,058,365-47,063,865Question Mark
    Overlapping variant regions from other studies: 193 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):44,584,736-44,590,236Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7011400Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1847,058,36547,063,865
    nsv7011400RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1844,584,73644,590,236

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18418188deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18418188Submitted genomicNC_000018.10:g.470
    58365_47063865del
    GRCh38 (hg38)NC_000018.10Chr1847,058,36547,063,865
    nssv18418188RemappedPerfectNC_000018.9:g.4458
    4736_44590236del
    GRCh37.p13First PassNC_000018.9Chr1844,584,73644,590,236

    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)
    nssv184181884e-061276238
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