A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625095



Internal ID6665247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1002638..1016158hg38UCSC Ensembl
chr11:1002638..1016158hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3813521
hg1913521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13992184, essv13992185
SamplesHG00251, HG03830
Known GenesAP2A2, MUC6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625095
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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