A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986552



Internal ID12978692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21223278..21302104hg38UCSC Ensembl
Innerchr3:21264770..21343596hg19UCSC Ensembl
Innerchr3:21239774..21318600hg18UCSC Ensembl
Innerchr3:21239774..21318600hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3878827
hg1978827
hg1878827
hg1778827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35115
Supporting Variants
SamplesNA11881
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986552
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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