A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518663



Internal ID20892024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47302163..47306898hg38UCSC Ensembl
chr18:44828534..44833269hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg384736
hg194736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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