A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699564



Internal ID123230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26720558..26720658hg38UCSC Ensembl
chr15:26965705..26965805hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496990
Supporting Variants
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699564
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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