A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981082



Internal ID12972780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4047125..4141990hg38UCSC Ensembl
Innerchr3:4088809..4183674hg19UCSC Ensembl
Innerchr3:4063809..4158674hg18UCSC Ensembl
Innerchr3:4063809..4158674hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3894866
hg1994866
hg1894866
hg1794866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752005
Supporting Variants
SamplesBEC_350
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981082
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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