A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194622



Internal ID20761662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23162501..23226400hg38UCSC Ensembl
chr15:22646668..22709832hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3863900
hg1963165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496310
Supporting Variants
Samples
Known GenesGOLGA8DP, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194622
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.04628


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