A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610665



Internal ID21802712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78920969..78923536hg38UCSC Ensembl
chr15:79213311..79215878hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382568
hg192568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031345
Supporting Variants
Samples
Known GenesCTSH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610665
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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