A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923079



Internal ID22698305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38665238..38665543hg38UCSC Ensembl
chr11:38686788..38687093hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923079
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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