A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595877



Internal ID16383286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160909586..161013330hg38UCSC Ensembl
Innerchr4:161830738..161934482hg19UCSC Ensembl
Innerchr4:162050188..162153932hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38103745
hg19103745
hg18103745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9345n54
Supporting Variantsnssv1153234
SamplesHGDP00774
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595877
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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