A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925185



Internal ID22700412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128926201..128927177hg38UCSC Ensembl
chr11:128796096..128797072hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925185
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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