A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917536



Internal ID22692755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128961088..128964896hg38UCSC Ensembl
chr11:128830983..128834791hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg383809
hg193809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357537
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917536
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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