A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533277



Internal ID20906638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33074365..33079561hg38UCSC Ensembl
chr19:33565271..33570467hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg385197
hg195197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533277
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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