A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11902185



Internal ID3824555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51909224..51932509hg38UCSC Ensembl
chr5:51205058..51228343hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3823286
hg1923286
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3605045
Supporting Variants
SamplesHG03461
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11902185
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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