A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202169



Internal ID20769209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12447801..12450900hg38UCSC Ensembl
chr20:12428449..12431548hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202169
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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