A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14088611



Internal ID4090427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34068151..34093059hg38UCSC Ensembl
chr11:34089698..34114606hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3824909
hg1924909
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625906
Supporting Variants
SamplesHG01522
Known GenesCAPRIN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14088611
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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