A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647456



Internal ID6687511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25285514..25296651hg38UCSC Ensembl
Innerchr22:25285561..25296604hg38UCSC Ensembl
Outerchr22:25285467..25296698hg38UCSC Ensembl
chr22:25681481..25692618hg19UCSC Ensembl
Innerchr22:25681528..25692571hg19UCSC Ensembl
Outerchr22:25681434..25692665hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3811138
hg1911138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16394677, essv16394678, essv16394679
SamplesNA19920, HG02420, NA18989
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647456
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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