A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16394679



Internal ID6396495
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647456
Supporting Variants
SamplesNA19920
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16394679
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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