A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990051



Internal ID60775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154502486..154505735hg38UCSC Ensembl
chr6:154823620..154826869hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg383250
hg193250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459917
Supporting Variants
Samples
Known GenesCNKSR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990051
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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