A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv706e199



Internal ID22758479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71945062..71956542hg38UCSC Ensembl
chr2:72172192..72183672hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3811481
hg1911481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2657764, esv2666808
SamplesHG00513
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv706e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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