A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625237



Internal ID7012072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5576678..5603099hg38UCSC Ensembl
chr11:5597908..5624329hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826422
hg1926422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14003810
SamplesHG01851
Known GenesOR52B6, TRIM6, TRIM6-TRIM34
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625237
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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