A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv620e214



Internal ID22756514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62943825..63005250hg38UCSC Ensembl
chr18:60611058..60672483hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3861426
hg1961426
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3642760, esv3642759, esv3642758
SamplesNA19725, HG00133, HG03907, HG00368, HG00373, HG04017, HG00366, HG02239
Known GenesPHLPP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv620e214
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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