A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13993603



Internal ID3995419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2303216..2328448hg38UCSC Ensembl
chr11:2324446..2349678hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3825233
hg1925233
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625125
Supporting Variants
SamplesHG02624
Known GenesTSPAN32
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13993603
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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