A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482122



Internal ID259583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11478401..11480469hg38UCSC Ensembl
chr10:11520400..11522468hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382069
hg192069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029154
Samples
Known GenesUSP6NL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482122
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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