A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533368



Internal ID20906729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32550353..32557970hg38UCSC Ensembl
chr18:30130316..30137933hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg387618
hg197618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533368
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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