A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv322e214



Internal ID18980497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18857379..18871546hg38UCSC Ensembl
chr13:19431519..19445686hg19UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3814168
hg1914168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3631366, esv3631367
SamplesHG01708
Known GenesANKRD20A9P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv322e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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