A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596096



Internal ID16383505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167847888..167907955hg38UCSC Ensembl
Innerchr4:168769039..168829106hg19UCSC Ensembl
Innerchr4:169005614..169065681hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3860068
hg1960068
hg1860068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1012866
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596096
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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