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nsv6330538

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:402

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 26 studies. See in: genome view    
    Submitted genomic70,249,903-70,250,304Question Mark
    Overlapping variant regions from other studies: 143 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):70,715,586-70,715,987Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6330538Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr170,249,90370,250,304
    nsv6330538RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr170,715,58670,715,987

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18063587deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18063587Submitted genomicNC_000001.11:g.702
    49903_70250304del
    GRCh38 (hg38)NC_000001.11Chr170,249,90370,250,304
    nssv18063587RemappedPerfectNC_000001.10:g.707
    15586_70715987del
    GRCh37.p13First PassNC_000001.10Chr170,715,58670,715,987

    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)
    nssv18063587<0.0013338750
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