A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987382



Internal ID12635179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17512143..17666270hg38UCSC Ensembl
Innerchr8:17369652..17523779hg19UCSC Ensembl
Innerchr8:17414033..17568059hg18UCSC Ensembl
Innerchr8:17414033..17568059hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38154128
hg19154128
hg18154027
hg17154027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34867
Supporting Variants
SamplesNA19012
Known GenesMTUS1, PDGFRL, SLC7A2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987382
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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