A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981926



Internal ID12974138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87704284..87751573hg38UCSC Ensembl
Innerchr4:88625436..88672725hg19UCSC Ensembl
Innerchr4:88844460..88891749hg18UCSC Ensembl
Innerchr4:88982615..89029904hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3847290
hg1947290
hg1847290
hg1747290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752051
Supporting Variants
SamplesBEC_501
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981926
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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