A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866659



Internal ID16160615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:5855566..5933152hg38UCSC Ensembl
Innerchr17:5758886..5836472hg19UCSC Ensembl
Innerchr17:5699610..5777196hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3877587
hg1977587
hg1877587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574308
Supporting Variants
Samples
Known GenesLOC339166
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866659
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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