A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179022



Internal ID20746062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39500690..39510431hg38UCSC Ensembl
chr15:39792891..39802632hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg389742
hg199742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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