A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029283



Internal ID20596323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27439972..27441895hg38UCSC Ensembl
chr16:27451293..27453216hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381924
hg191924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496624
Supporting Variants
Samples
Known GenesIL21R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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