A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv614e214



Internal ID20122037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46702717..46833888hg38UCSC Ensembl
chr18:44282680..44413851hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38131172
hg19131172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3642439, esv3642440
SamplesHG02140, HG00651, HG02016, HG03743, HG04212, HG03738, HG03978, HG03837
Known GenesPIAS2, ST8SIA5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv614e214
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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