A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv864085



Internal ID15811355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:168683..171713hg38UCSC Ensembl
Innerchr17:18474..21504hg19UCSC Ensembl
Innerchr17:18474..21504hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg383031
hg193031
hg183031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573866
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)nssv864085
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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