A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13412053



Internal ID3413869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17265406..17284899hg38UCSC Ensembl
Innerchr9:17265406..17284899hg38UCSC Ensembl
Outerchr9:17264906..17285399hg38UCSC Ensembl
chr9:17265404..17284897hg19UCSC Ensembl
Innerchr9:17265404..17284897hg19UCSC Ensembl
Outerchr9:17264904..17285397hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3819494
hg1919494
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619837
Supporting Variants
SamplesHG03689
Known GenesCNTLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13412053
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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