A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978240



Internal ID12981629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:49545588..49607488hg38UCSC Ensembl
Innerchr8:50458147..50520047hg19UCSC Ensembl
Innerchr8:50620700..50682600hg18UCSC Ensembl
Innerchr8:50620700..50682600hg17UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3861901
hg1961901
hg1861901
hg1761901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34964
Supporting Variants
SamplesNA18990
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978240
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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