A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv323e214



Internal ID22756217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21207202..21219686hg38UCSC Ensembl
chr13:21781341..21793825hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3812485
hg1912485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3631458, esv3631457
SamplesHG04212, HG00142, NA19917, HG03990, NA18630, HG01607, HG03971, HG03969, HG03949, HG04015, HG03882, HG00628
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv323e214
Frequency
Sample Size2504
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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