A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988006



Internal ID12972569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3986195..4107492hg38UCSC Ensembl
Innerchr3:4027879..4149176hg19UCSC Ensembl
Innerchr3:4002879..4124176hg18UCSC Ensembl
Innerchr3:4002879..4124176hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38121298
hg19121298
hg18121298
hg17121298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752004
Supporting Variants
SamplesBEC_328
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988006
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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