A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918204



Internal ID22693425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19159517..19161733hg38UCSC Ensembl
chr11:19181064..19183280hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382217
hg192217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360451
Samples
Known GenesZDHHC13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918204
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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