A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981976



Internal ID12627545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4124045..4198166hg38UCSC Ensembl
Innerchr3:4165729..4239850hg19UCSC Ensembl
Innerchr3:4140729..4214850hg18UCSC Ensembl
Innerchr3:4140729..4214850hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3874122
hg1974122
hg1874122
hg1774122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752006
Supporting Variants
SamplesBEC_51
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981976
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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