A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143682



Internal ID342883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45828265..45842265hg38UCSC Ensembl
chr10:46323713..46337713hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3814001
hg1914001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17034495
Samples
Known GenesAGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143682
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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