A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990323



Internal ID60952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165619308..165619421hg38UCSC Ensembl
chr6:166032796..166032909hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458313
Supporting Variants
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990323
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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