A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186566



Internal ID20753606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66810210..66810634hg38UCSC Ensembl
chr15:67102548..67102972hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510995
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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