A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981266



Internal ID12973077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8794854..8854946hg38UCSC Ensembl
Innerchr3:8836540..8896630hg19UCSC Ensembl
Innerchr3:8811540..8871630hg18UCSC Ensembl
Innerchr3:8811540..8871630hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3860093
hg1960091
hg1860091
hg1760091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752019
Supporting Variants
SamplesBEC_375
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981266
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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