A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596167



Internal ID16383576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170655143..170750887hg38UCSC Ensembl
Innerchr4:171576294..171672038hg19UCSC Ensembl
Innerchr4:171812869..171908613hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3895745
hg1995745
hg1895745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1013116
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596167
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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