A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382816



Internal ID22440686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27224850..27226642hg38UCSC Ensembl
chr15:27469997..27471789hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381793
hg191793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945522
Supporting Variants
Samples
Known GenesGABRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382816
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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