A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592208



Internal ID16379617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162652075..162719314hg38UCSC Ensembl
Innerchr3:162369863..162437102hg19UCSC Ensembl
Innerchr3:163852557..163919796hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3867240
hg1967240
hg1867240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv977592
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592208
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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