A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203896



Internal ID20770936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56732791..56736141hg38UCSC Ensembl
chr20:55307847..55311197hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg383351
hg193351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540468
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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