A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520234



Internal ID20893595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24811304..24811872hg38UCSC Ensembl
chr18:22391268..22391836hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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