A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625366



Internal ID7012200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10942118..10963657hg38UCSC Ensembl
chr11:10963665..10985204hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3821540
hg1921540
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv185e214
Supporting Variantsessv14029101, essv14029098, essv14029093, essv14029097, essv14029099, essv14029094, essv14029095, essv14029096, essv14029092, essv14029102, essv14029100, essv14029091
SamplesHG03517, NA19171, NA19131, HG03267, NA19209, HG02009, NA19440, NA19331, NA19334, NA19428, HG03157, NA20334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625366
Frequency
Sample Size2504
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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