A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958213



Internal ID39457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157317716..157414598hg38UCSC Ensembl
chr4:158238868..158335750hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3896883
hg1996883
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470431
Supporting Variants
Samples
Known GenesGRIA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958213
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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