A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490332



Internal ID267588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12200653..12828405hg38UCSC Ensembl
chr10:12242652..12870404hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38627753
hg19627753
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029232
Samples
Known GenesCAMK1D, CDC123, MIR4480
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490332
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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