A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv326e214



Internal ID22756220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32816802..32876071hg38UCSC Ensembl
chr13:33390940..33450209hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3859270
hg1959270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3631730, esv3631729
SamplesNA19445, NA19360
Known GenesLINC00423
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv326e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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