A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203802



Internal ID20770842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17346946..17682654hg38UCSC Ensembl
chr21:18719265..19054972hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38335709
hg19335708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542916
Supporting Variants
Samples
Known GenesBTG3, C21orf37, CXADR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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