A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv341e214



Internal ID22756235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66650981..66753143hg38UCSC Ensembl
chr13:67225113..67327275hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38102163
hg19102163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3632518, esv3632516, esv3632520
SamplesNA18592, NA20849
Known GenesPCDH9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv341e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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