A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919979



Internal ID22695202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9315241..9315718hg38UCSC Ensembl
chr11:9336788..9337265hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919979
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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