A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521565



Internal ID20894926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23455505..23462262hg38UCSC Ensembl
chr18:21035469..21042226hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg386758
hg196758
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186118
Samples
Known GenesRIOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521565
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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