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nsv4601783

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:956

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 185 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):10,407,373-10,408,328Question Mark
    Overlapping variant regions from other studies: 186 SVs from 39 studies. See in: genome view    
    Submitted genomic10,559,972-10,560,927Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
    nsv4601783RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1210,407,37310,408,328
    nsv4601783Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1210,559,97210,560,927

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv16146940deletionCuratedCurated

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
    nssv16146940RemappedPerfectNC_000012.12:g.(?_
    10407373)_(1040832
    8_?)del
    GRCh38.p12First PassNC_000012.12Chr1210,407,37310,408,328
    nssv16146940Submitted genomicNC_000012.11:g.(?_
    10559972)_(1056092
    7_?)del
    GRCh37 (hg19)NC_000012.11Chr1210,559,97210,560,927

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv161469400.0011845
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