A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872796



Internal ID15820066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46474739..46529499hg38UCSC Ensembl
Innerchr17:44552105..44606865hg19UCSC Ensembl
Innerchr17:41907421..41962181hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3854761
hg1954761
hg1854761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575374
Supporting Variants
Samples
Known GenesARL17A, LRRC37A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv872796
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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