A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv632e214



Internal ID20122055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69875833..69891905hg38UCSC Ensembl
chr18:67543069..67559141hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3816073
hg1916073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3642978, esv3642979
SamplesNA06984, HG03947, HG03061
Known GenesCD226
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv632e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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