A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914341



Internal ID22689558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17080943..17082028hg38UCSC Ensembl
chr11:17102490..17103575hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914341
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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