A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294792



Internal ID20504010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26764149..26764201hg38UCSC Ensembl
chr15:27009296..27009348hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744653
Supporting Variants
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294792
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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