A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187765



Internal ID20754805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11869019..11881076hg38UCSC Ensembl
chr16:11962876..11974933hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3812058
hg1912058
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497385
Supporting Variants
Samples
Known GenesGSPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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