A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988050



Internal ID12979159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48381200..48908580hg38UCSC Ensembl
Innerchr11:48402752..48930132hg19UCSC Ensembl
Innerchr11:48359328..48886708hg18UCSC Ensembl
Innerchr11:48359328..48886708hg17UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38527381
hg19527381
hg18527381
hg17527381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34690
Supporting Variants
SamplesNA12707
Known GenesOR4A47
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988050
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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