A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923876



Internal ID22699103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65805827..65812874hg38UCSC Ensembl
chr11:65573298..65580345hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387048
hg197048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923876
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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