A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926677



Internal ID22701904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65215899..65216217hg38UCSC Ensembl
chr11:64983370..64983688hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369530
Samples
Known GenesSLC22A20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926677
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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