A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626471



Internal ID7013303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56053534..56249437hg38UCSC Ensembl
chr11:55821010..56016913hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38195904
hg19195904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv200e214
Supporting Variantsessv14165831, essv14165832
SamplesHG03563, HG01620
Known GenesOR5J2, OR5T2, OR8H2, OR8H3, OR8I2, OR8J3, OR8K5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626471
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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