A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488628



Internal ID265932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88640529..88658071hg38UCSC Ensembl
chr10:90400286..90417828hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3817543
hg1917543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488628
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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