A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16413536



Internal ID5329473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36080820..36085231hg38UCSC Ensembl
Innerchr22:36080820..36085231hg38UCSC Ensembl
Outerchr22:36080527..36085595hg38UCSC Ensembl
chr22:36476868..36481279hg19UCSC Ensembl
Innerchr22:36476868..36481279hg19UCSC Ensembl
Outerchr22:36476575..36481643hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg384412
hg194412
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647676
Supporting Variants
SamplesNA18871
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16413536
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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