A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv864089



Internal ID15811359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:169598..181019hg38UCSC Ensembl
Innerchr17:19389..30810hg19UCSC Ensembl
Innerchr17:19389..30810hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3811422
hg1911422
hg1811422
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573869
Supporting Variants
Samples
Known GenesDOC2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv864089
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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