A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981083



Internal ID12972767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4064816..4092556hg38UCSC Ensembl
Innerchr3:4106500..4134240hg19UCSC Ensembl
Innerchr3:4081500..4109240hg18UCSC Ensembl
Innerchr3:4081500..4109240hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3827741
hg1927741
hg1827741
hg1727741
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)essv6981083
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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