A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647936



Internal ID7034675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45651925..45671680hg38UCSC Ensembl
Innerchr22:45651938..45671668hg38UCSC Ensembl
Outerchr22:45651913..45671693hg38UCSC Ensembl
chr22:46047805..46067560hg19UCSC Ensembl
Innerchr22:46047818..46067548hg19UCSC Ensembl
Outerchr22:46047793..46067573hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3819756
hg1919756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16444860
SamplesHG02339
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647936
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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