A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619884



Internal ID7006758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18833106..18856929hg38UCSC Ensembl
chr9:18833104..18856927hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3823824
hg1923824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13415192
SamplesNA20795
Known GenesADAMTSL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619884
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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