A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186377



Internal ID20753417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78534875..78557953hg38UCSC Ensembl
chr15:78827217..78850295hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3823079
hg1923079
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497813
Supporting Variants
Samples
Known GenesHYKK, PSMA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186377
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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