A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16411314



Internal ID4757686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34899153..34901485hg38UCSC Ensembl
Innerchr22:34899202..34901437hg38UCSC Ensembl
Outerchr22:34899105..34901534hg38UCSC Ensembl
chr22:35295144..35297476hg19UCSC Ensembl
Innerchr22:35295193..35297428hg19UCSC Ensembl
Outerchr22:35295096..35297525hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382333
hg192333
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647653
Supporting Variants
SamplesNA10851
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16411314
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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