A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6070696



Internal ID8846582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:43152910..43157516hg38UCSC Ensembl
Outerchr22:43152539..43157886hg38UCSC Ensembl
Innerchr22:43548916..43553522hg19UCSC Ensembl
Outerchr22:43548545..43553892hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg385348
hg195348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671621
Supporting Variants
SamplesHG00282
Known GenesTSPO
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6070696
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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