A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184605



Internal ID20751645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47898436..47911621hg38UCSC Ensembl
chr16:47932347..47945532hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3813186
hg1913186
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507017
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184605
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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