A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071793



Internal ID20638833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29026250..29029142hg38UCSC Ensembl
chr21:30398571..30401463hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg382893
hg192893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539369
Supporting Variants
Samples
Known GenesUSP16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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