A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925010



Internal ID22700237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119417464..119417519hg38UCSC Ensembl
chr11:119288174..119288229hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355249
Samples
Known GenesUSP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925010
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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