A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14003810



Internal ID2000480
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625237
Supporting Variants
SamplesHG01851
Known GenesOR52B6, TRIM6, TRIM6-TRIM34
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14003810
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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