A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988005



Internal ID12972570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3979832..4124049hg38UCSC Ensembl
Innerchr3:4021516..4165733hg19UCSC Ensembl
Innerchr3:3996516..4140733hg18UCSC Ensembl
Innerchr3:3996516..4140733hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38144218
hg19144218
hg18144218
hg17144218
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)essv6988005
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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