A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14015563



Internal ID4017379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7666840..7787334hg38UCSC Ensembl
chr11:7688071..7808881hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38120495
hg19120811
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625297
Supporting Variants
SamplesHG01435
Known GenesCYB5R2, OVCH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14015563
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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