A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790823



Internal ID18831027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4668512..4974456hg38UCSC Ensembl
Innerchr11:4689742..4995686hg19UCSC Ensembl
Innerchr11:4646318..4952262hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38305945
hg19305945
hg18305945
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891914
Supporting Variants
Samples
Known GenesOR51A2, OR51A4, OR51A7, OR51E2, OR51F1, OR51F2, OR51G1, OR51G2, OR51S1, OR51T1, OR52R1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=129
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790823
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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