A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16413435



Internal ID441202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35737423..35738203hg38UCSC Ensembl
Innerchr22:35737425..35738202hg38UCSC Ensembl
Outerchr22:35737422..35738205hg38UCSC Ensembl
chr22:36133470..36134250hg19UCSC Ensembl
Innerchr22:36133472..36134249hg19UCSC Ensembl
Outerchr22:36133469..36134252hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647673
Supporting Variants
SamplesHG00137
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16413435
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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