A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980227



Internal ID12981465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:49519454..49607471hg38UCSC Ensembl
Innerchr8:50432013..50520030hg19UCSC Ensembl
Innerchr8:50594566..50682583hg18UCSC Ensembl
Innerchr8:50594566..50682583hg17UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3888018
hg1988018
hg1888018
hg1788018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34838
Supporting Variants
SamplesNA18970
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980227
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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