A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925923



Internal ID22701150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124765979..124766029hg38UCSC Ensembl
chr11:124635875..124635925hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925923
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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