A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14043397



Internal ID1662188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18641418..18666038hg38UCSC Ensembl
chr11:18662965..18687585hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3824621
hg1924621
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625508
Supporting Variants
SamplesHG01525
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14043397
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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