A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182327



Internal ID20749367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30992201..30998200hg38UCSC Ensembl
chr15:31284404..31290403hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182327
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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