A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699565



Internal ID123231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26737358..26738588hg38UCSC Ensembl
chr15:26982505..26983735hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505643
Supporting Variants
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699565
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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