A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989584



Internal ID60484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146282362..146282364hg38UCSC Ensembl
chr6:146603498..146603500hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543556
Supporting Variants
Samples
Known GenesGRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989584
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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