A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6029536



Internal ID9441764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31641542..31642828hg38UCSC Ensembl
chr22:32037528..32038814hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381287
hg191287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665358
Supporting Variants
SamplesNA18853
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6029536
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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