A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699568



Internal ID123234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26766602..26766808hg38UCSC Ensembl
chr15:27011749..27011955hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513401
Supporting Variants
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699568
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003746


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