A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206658



Internal ID20773698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32720165..32722140hg38UCSC Ensembl
chr21:34092475..34094450hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381976
hg191976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552005
Supporting Variants
Samples
Known GenesSYNJ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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