A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596055



Internal ID16383464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:166161405..166199789hg38UCSC Ensembl
Innerchr4:167082557..167120941hg19UCSC Ensembl
Innerchr4:167302007..167340391hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3838385
hg1938385
hg1838385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1012717
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596055
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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