A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923538



Internal ID22698765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125507201..125507522hg38UCSC Ensembl
chr11:125377097..125377418hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923538
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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