A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528076



Internal ID20901437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55645706..55655461hg38UCSC Ensembl
chr18:53312937..53322692hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg389756
hg199756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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