A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35159



Internal ID12644509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167885235..168058165hg38UCSC Ensembl
Innerchr4:168806386..168979316hg19UCSC Ensembl
Innerchr4:169042961..169215891hg18UCSC Ensembl
Innerchr4:169181116..169354046hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38172931
hg19172931
hg18172931
hg17172931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv194e55
Supporting Variantsessv6978023, essv6978022
SamplesNA10857
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv35159
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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