A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16402286



Internal ID6404102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30060553..30066387hg38UCSC Ensembl
chr22:30456542..30462376hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg385835
hg195835
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647555
Supporting Variants
SamplesHG02654
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16402286
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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