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nsv7004703

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:723

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 26 studies. See in: genome view    
    Submitted genomic48,821,948-48,822,670Question Mark
    Overlapping variant regions from other studies: 90 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):49,325,205-49,325,927Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7004703Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,821,94848,822,670
    nsv7004703RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,325,20549,325,927

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18424040deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18424040Submitted genomicNC_000019.10:g.488
    21948_48822670del
    GRCh38 (hg38)NC_000019.10Chr1948,821,94848,822,670
    nssv18424040RemappedPerfectNC_000019.9:g.4932
    5205_49325927del
    GRCh37.p13First PassNC_000019.9Chr1949,325,20549,325,927

    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)
    nssv184240404e-061270924
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