A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913540



Internal ID22688756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96581434..96581541hg38UCSC Ensembl
chr11:96452432..96452540hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38108
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913540
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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