A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341348



Internal ID20998901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102001901..102003900hg38UCSC Ensembl
chr2:102618363..102620362hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205776
Samples
Known GenesIL1R2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341348
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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