A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626473



Internal ID7013305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56075119..56173453hg38UCSC Ensembl
chr11:55842595..55940929hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3898335
hg1998335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14165838, essv14165837, essv14165836
SamplesHG00346, HG03563, HG00371
Known GenesOR8H2, OR8H3, OR8I2, OR8J3, OR8K5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626473
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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