A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918272



Internal ID22693493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14454111..14454370hg38UCSC Ensembl
chr11:14475657..14475916hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918272
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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