A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519075



Internal ID20892436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63287432..63288059hg38UCSC Ensembl
chr18:60954665..60955292hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043399
Samples
Known GenesBCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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