A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978847



Internal ID12979207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17701447..17793406hg38UCSC Ensembl
Innerchr5:17701556..17793515hg19UCSC Ensembl
Innerchr5:17734268..17829272hg18UCSC Ensembl
Innerchr5:17734268..17829272hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3891960
hg1991960
hg1895005
hg1795005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35046
Supporting Variants
SamplesNA12740
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978847
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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