A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486728



Internal ID264086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62908608..62908733hg38UCSC Ensembl
chr10:64668368..64668493hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17034015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486728
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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