A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526679



Internal ID20900040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23242204..23251494hg38UCSC Ensembl
chr18:20822168..20831458hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg389291
hg199291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040363
Samples
Known GenesCABLES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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