A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199364



Internal ID20766404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28250566..28611740hg38UCSC Ensembl
chr19:28741473..29102647hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38361175
hg19361175
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199364
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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