A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203803



Internal ID20770843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17364529..17766164hg38UCSC Ensembl
chr21:18736848..19138481hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38401636
hg19401634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535650
Supporting Variants
Samples
Known GenesBTG3, C21orf37, CXADR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203803
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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