A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595876



Internal ID16383285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160909586..161011850hg38UCSC Ensembl
Innerchr4:161830738..161933002hg19UCSC Ensembl
Innerchr4:162050188..162152452hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38102265
hg19102265
hg18102265
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9345n54
Supporting Variantsnssv1153233
SamplesHGDP00762
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595876
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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