A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193486



Internal ID20760526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12524845..12530842hg38UCSC Ensembl
chr16:12618702..12624699hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg385998
hg195998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498449
Supporting Variants
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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