A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981721



Internal ID12972587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3981366..4092556hg38UCSC Ensembl
Innerchr3:4023050..4134240hg19UCSC Ensembl
Innerchr3:3998050..4109240hg18UCSC Ensembl
Innerchr3:3998050..4109240hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38111191
hg19111191
hg18111191
hg17111191
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981721
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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