A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979608



Internal ID12980444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152707769..152763786hg38UCSC Ensembl
Innerchr3:152425558..152481575hg19UCSC Ensembl
Innerchr3:153908248..153964265hg18UCSC Ensembl
Innerchr3:153908256..153964273hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3856018
hg1956018
hg1856018
hg1756018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34910
Supporting Variants
SamplesNA18579
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979608
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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