A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16413109



Internal ID3460331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35596755..35597550hg38UCSC Ensembl
Innerchr22:35596805..35597500hg38UCSC Ensembl
Outerchr22:35596662..35597643hg38UCSC Ensembl
chr22:35992802..35993597hg19UCSC Ensembl
Innerchr22:35992852..35993547hg19UCSC Ensembl
Outerchr22:35992709..35993690hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647666
Supporting Variants
SamplesHG03082
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16413109
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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