A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595873



Internal ID6636147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36722692..36724698hg38UCSC Ensembl
Innerchr3:36722692..36724698hg38UCSC Ensembl
Outerchr3:36722434..36724897hg38UCSC Ensembl
chr3:36764183..36766189hg19UCSC Ensembl
Innerchr3:36764183..36766189hg19UCSC Ensembl
Outerchr3:36763925..36766388hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382007
hg192007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10981037, essv10981038, essv10981036
SamplesNA19678, HG03940, HG01105
Known GenesDCLK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595873
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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