A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573878



Internal ID16014601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:170860..180780hg38UCSC Ensembl
Innerchr17:20651..30571hg19UCSC Ensembl
Innerchr17:20651..30571hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg389921
hg199921
hg189921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5347n54
Supporting Variantsnssv864144
Samples
Known GenesDOC2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573878
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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