A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv864205



Internal ID15811475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:171764..181157hg38UCSC Ensembl
Innerchr17:21555..30948hg19UCSC Ensembl
Innerchr17:21555..30948hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg389394
hg199394
hg189394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573902
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)nssv864205
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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