A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619837



Internal ID6660023
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13412053, essv13412054
SamplesNA18539, HG03689
Known GenesCNTLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619837
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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