A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988562



Internal ID59801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101583456..101585584hg38UCSC Ensembl
chr6:102031331..102033459hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg382129
hg192129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457795
Supporting Variants
Samples
Known GenesGRIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988562
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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