A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184855



Internal ID20751895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8896082..9128062hg38UCSC Ensembl
chr16:8989939..9221919hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38231981
hg19231981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501975
Supporting Variants
Samples
Known GenesC16orf72, USP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184855
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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