A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14079531



Internal ID4081347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31829189..31844684hg38UCSC Ensembl
chr11:31850736..31866230hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3815496
hg1915495
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625840
Supporting Variants
SamplesHG01447
Known GenesDKFZp686K1684
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14079531
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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