A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv653e214



Internal ID18980828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11894255..11919495hg38UCSC Ensembl
chr19:12005070..12030310hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3825241
hg1925241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3643680, esv3643681
SamplesNA20785
Known GenesZNF69
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv653e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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