A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv211e214



Internal ID20121634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78524451..78661281hg38UCSC Ensembl
chr11:78235497..78372326hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38136831
hg19136830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3626902, esv3626903
SamplesHG00142, HG02784, HG03895, HG03837, HG03644, HG03672, HG03019, NA20888, NA20852, HG02778, HG03989
Known GenesNARS2, TENM4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv211e214
Frequency
Sample Size2504
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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