A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978404



Internal ID12981923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55609530..55853223hg38UCSC Ensembl
Innerchr11:55377006..55620699hg19UCSC Ensembl
Innerchr11:55133582..55377275hg18UCSC Ensembl
Innerchr11:55133582..55377275hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38243694
hg19243694
hg18243694
hg17243694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34793
Supporting Variants
SamplesNA19093
Known GenesOR4C6, OR4P4, OR4S2, OR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978404
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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