A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625296



Internal ID6665444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7635550..7688660hg38UCSC Ensembl
chr11:7656781..7709891hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3853111
hg1953111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14015562
SamplesHG01853
Known GenesCYB5R2, PPFIBP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625296
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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