A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505779



Internal ID18804060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5772199..5788096hg38UCSC Ensembl
Innerchr11:5793429..5809326hg19UCSC Ensembl
Innerchr11:5750005..5765902hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3815898
hg1915898
hg1815898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039281
Supporting Variants
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3505779
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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