A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466482



Internal ID244318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165329839..165330304hg38UCSC Ensembl
chr6:165743328..165743793hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990311
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466482
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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