A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912391



Internal ID22687607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68299740..68301782hg38UCSC Ensembl
chr11:68067208..68069250hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382043
hg192043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912391
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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