A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922459



Internal ID22697684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128210664..128210903hg38UCSC Ensembl
chr11:128080559..128080798hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922459
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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