A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv185e214



Internal ID22756079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10942118..10964251hg38UCSC Ensembl
chr11:10963665..10985798hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3822134
hg1922134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3625367, esv3625366
SamplesHG00142, HG03517, NA19171, NA19131, HG00610, HG00182, HG03267, NA19209, HG02009, HG03363, NA19440, NA19331, NA19334, NA19428, HG03157, NA20334, HG00628
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv185e214
Frequency
Sample Size2504
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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