A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv864169



Internal ID15811439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:170860..181795hg38UCSC Ensembl
Innerchr17:20651..31586hg19UCSC Ensembl
Innerchr17:20651..31586hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3810936
hg1910936
hg1810936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573887
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)nssv864169
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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