A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14165838



Internal ID3909929
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626473
Supporting Variants
SamplesHG03563
Known GenesOR8H2, OR8H3, OR8I2, OR8J3, OR8K5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14165838
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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