A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560426



Internal ID18512021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16897474..16965546hg38UCSC Ensembl
Innerchr17:16800788..16868860hg19UCSC Ensembl
Innerchr17:16741513..16809585hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3868073
hg1968073
hg1868073
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055688
Supporting Variants
Samples
Known GenesTNFRSF13B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560426
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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