A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv381e199



Internal ID22758154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112670699..112672095hg38UCSC Ensembl
chr13:113325013..113326409hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381397
hg191397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2674970, esv2661827
SamplesNA11829, NA18861, NA19704, NA19819, NA18489, NA19152, NA19391, NA18853, NA19318, NA18909, NA18873, NA19116, NA19900, NA18505
Known GenesC13orf35
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv381e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer