A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990311



Internal ID60942
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 StatusS
Merged Variantsnsv5466482
Supporting Variants
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990311
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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