A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029379



Internal ID20596419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3489101..3498500hg38UCSC Ensembl
chr16:3539101..3548500hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514045
Supporting Variants
Samples
Known GenesC16orf90
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00051


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