A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv636e214



Internal ID22756530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71614930..71680489hg38UCSC Ensembl
chr18:69282166..69347725hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3865560
hg1965560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3643024, esv3643025
SamplesNA06984, HG03061, HG03397, HG00329
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv636e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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