A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528803



Internal ID20902164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63084152..63089265hg38UCSC Ensembl
chr18:60751385..60756498hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg385114
hg195114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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