A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785067



Internal ID18827271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5081246..5227774hg38UCSC Ensembl
Innerchr11:5102476..5249004hg19UCSC Ensembl
Innerchr11:5059052..5205580hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38146529
hg19146529
hg18146529
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891917
Supporting Variants
Samples
Known GenesHBB, OR51V1, OR52A1, OR52A5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=46
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785067
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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