A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203294



Internal ID20770334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33759519..33761499hg38UCSC Ensembl
chr20:32347325..32349305hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517344
Supporting Variants
Samples
Known GenesZNF341
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203294
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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