A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534978



Internal ID20908339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58775055..58775360hg38UCSC Ensembl
chr18:56442287..56442592hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534978
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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