A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513139



Internal ID18464734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55588246..55641874hg38UCSC Ensembl
Innerchr11:55355722..55409350hg19UCSC Ensembl
Innerchr11:55112298..55165926hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3853629
hg1953629
hg1853629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041523
Supporting Variants
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513139
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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