A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989021



Internal ID12981929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55677848..55783448hg38UCSC Ensembl
Innerchr11:55445324..55550924hg19UCSC Ensembl
Innerchr11:55201900..55307500hg18UCSC Ensembl
Innerchr11:55201900..55307500hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38105601
hg19105601
hg18105601
hg17105601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35012
Supporting Variants
SamplesNA19094
Known GenesOR5D13
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989021
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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