A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179375



Internal ID20746415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75176093..75222033hg38UCSC Ensembl
chr16:75209991..75255931hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3845941
hg1945941
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501729
Supporting Variants
Samples
Known GenesCTRB1, CTRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179375
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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