A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179435



Internal ID20746475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48092841..48106505hg38UCSC Ensembl
chr16:48126752..48140416hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3813665
hg1913665
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502408
Supporting Variants
Samples
Known GenesABCC12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179435
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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