A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596557



Internal ID16383966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189784978..189916895hg38UCSC Ensembl
Innerchr4:190706132..190838050hg19UCSC Ensembl
Innerchr4:190943126..191075044hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38131918
hg19131919
hg18131919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1020875
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596557
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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