A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592615



Internal ID16380024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176236398..176282631hg38UCSC Ensembl
Innerchr3:175954186..176000419hg19UCSC Ensembl
Innerchr3:177436880..177483113hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3846234
hg1946234
hg1846234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv981623
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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