A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485351



Internal ID262742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115168..187666hg38UCSC Ensembl
chr10:161108..233606hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3872499
hg1972499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029830
Samples
Known GenesZMYND11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485351
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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