A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522157



Internal ID20895518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63122283..63128272hg38UCSC Ensembl
chr18:60789516..60795505hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg385990
hg195990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043393
Samples
Known GenesBCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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