A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520605



Internal ID20893966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69233065..69233320hg38UCSC Ensembl
chr18:66900302..66900557hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520605
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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