A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926724



Internal ID22701951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128450201..128452353hg38UCSC Ensembl
chr11:128320096..128322248hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382153
hg192153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926724
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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