A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595922



Internal ID16383331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161019278..161080755hg38UCSC Ensembl
Innerchr4:161940430..162001907hg19UCSC Ensembl
Innerchr4:162159880..162221357hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3861478
hg1961478
hg1861478
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9351n54
Supporting Variantsnssv1010246
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595922
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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