A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063963



Internal ID19153182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6229480hg38UCSC Ensembl
Innerchr17:6106486..6132800hg19UCSC Ensembl
Innerchr17:6047210..6073524hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3826315
hg1926315
hg1826315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3091n100
Supporting Variantsnssv3560270, nssv3560254, nssv3560251, nssv3560275, nssv3560230, nssv3560223, nssv3560240, nssv3560199, nssv3560238, nssv3560231, nssv3560268, nssv3560213, nssv3560242, nssv3560253, nssv3560207, nssv3560277, nssv3560239, nssv3560233, nssv3560206, nssv3560243, nssv3560209, nssv3560266, nssv3560201, nssv3560196, nssv3560280, nssv3560245, nssv3560235, nssv3560221, nssv3560273, nssv3560262, nssv3560211, nssv3560228, nssv3560250, nssv3560264, nssv3560259, nssv3560234, nssv3560241, nssv3560278, nssv3560216, nssv3560229, nssv3560215, nssv3560248, nssv3560255, nssv3560214, nssv3560218, nssv3560212, nssv3560267, nssv3560225, nssv3560274, nssv3560244, nssv3560202, nssv3560236, nssv3560237, nssv3560200, nssv3560261, nssv3560276, nssv3560279, nssv3560265, nssv3560227, nssv3560226, nssv3560203, nssv3560205, nssv3560257, nssv3560219, nssv3560246, nssv3560256, nssv3560222, nssv3560198, nssv3560224, nssv3560263, nssv3560220, nssv3560204, nssv3560258, nssv3560271, nssv3560210, nssv3560252, nssv3560208, nssv3560249, nssv3560232, nssv3560272, nssv3560197, nssv3560217, nssv3560260, nssv3560269, nssv3560247
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063963
Frequency
Sample Size11257
Observed Gain0
Observed Loss85
Observed Complex0
Frequencyn/a


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