A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978023



Internal ID12631806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167893119..168058119hg38UCSC Ensembl
Innerchr4:168814270..168979270hg19UCSC Ensembl
Innerchr4:169050845..169215845hg18UCSC Ensembl
Innerchr4:169189000..169354000hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38165001
hg19165001
hg18165001
hg17165001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35159
Supporting Variants
SamplesNA10857
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978023
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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