A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533484



Internal ID20906845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:52297125..52297760hg38UCSC Ensembl
chr18:49823495..49824130hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041555
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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