A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1071e214



Internal ID22756965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11165930..11179810hg38UCSC Ensembl
chr5:11166042..11179922hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3813881
hg1913881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3604016, esv3604017
SamplesHG04001, HG04206, HG04180, HG03823, NA19467, NA19316, HG02060, HG03886
Known GenesCTNND2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1071e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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