A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525811



Internal ID20899172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26450503..26452538hg38UCSC Ensembl
chr18:24030467..24032502hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382036
hg192036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525811
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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