A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987730



Internal ID12981379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104436466..105059466hg38UCSC Ensembl
Innerchr3:104155310..104778310hg19UCSC Ensembl
Innerchr3:105638000..106261000hg18UCSC Ensembl
Innerchr3:105638000..106261000hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38623001
hg19623001
hg18623001
hg17623001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35023
Supporting Variants
SamplesNA18966
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987730
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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