A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981720



Internal ID12972572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3979832..4163939hg38UCSC Ensembl
Innerchr3:4021516..4205623hg19UCSC Ensembl
Innerchr3:3996516..4180623hg18UCSC Ensembl
Innerchr3:3996516..4180623hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38184108
hg19184108
hg18184108
hg17184108
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)essv6981720
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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