A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625125



Internal ID7011963
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13993601, essv13993602, essv13993603
SamplesHG02583, HG02624, HG01142
Known GenesTSPAN32
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625125
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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