A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990938



Internal ID61374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163489425..163489665hg38UCSC Ensembl
chr6:163910457..163910697hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465388
Supporting Variants
Samples
Known GenesQKI
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990938
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006244


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