A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv124e199



Internal ID22757897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21396151..21398316hg38UCSC Ensembl
chr10:21685080..21687245hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg382166
hg192166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2675070, esv2661682
SamplesNA20778, HG00342, HG00310, NA20772
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv124e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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