A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10981038



Internal ID982854
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595873
Supporting Variants
SamplesNA19678
Known GenesDCLK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10981038
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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