A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029909



Internal ID20596949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4837208..4842767hg38UCSC Ensembl
chr16:4887209..4892768hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385560
hg195560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500647
Supporting Variants
Samples
Known GenesGLYR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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