A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184537



Internal ID20751577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13167107..13170794hg38UCSC Ensembl
chr16:13260964..13264651hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg383688
hg193688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503651
Supporting Variants
Samples
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184537
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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