A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986570



Internal ID58484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101782623..101784500hg38UCSC Ensembl
chr6:102230498..102232375hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460317
Supporting Variants
Samples
Known GenesGRIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986570
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer