A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv368e214



Internal ID22756262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106299348..106337573hg38UCSC Ensembl
chr13:106951697..106989921hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3838226
hg1938225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3633463, esv3633461
SamplesHG03118
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv368e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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