A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14210774



Internal ID4367916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72150936..72178148hg38UCSC Ensembl
chr11:71861980..71889192hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3827213
hg1927213
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626793
Supporting Variants
SamplesHG03898
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14210774
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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