A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978759



Internal ID12632383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14908020..15015420hg38UCSC Ensembl
Innerchr8:14765529..14872929hg19UCSC Ensembl
Innerchr8:14809900..14917300hg18UCSC Ensembl
Innerchr8:14809900..14917300hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38107401
hg19107401
hg18107401
hg17107401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34951
Supporting Variants
SamplesNA12234
Known GenesSGCZ
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978759
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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