A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982963



Internal ID21892306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23898901..23906629hg38UCSC Ensembl
chr1:24225391..24233119hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg387729
hg197729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536196
Samples
Known GenesCNR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982963
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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