A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192908



Internal ID20759948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39503686..39508237hg38UCSC Ensembl
chr15:39795887..39800438hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384552
hg194552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499468
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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