A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918859



Internal ID22694081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62408910..62410885hg38UCSC Ensembl
chr11:62176382..62178357hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381976
hg191976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918859
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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