A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917431



Internal ID22692650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119434130..119435264hg38UCSC Ensembl
chr11:119304840..119305974hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381135
hg191135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354425
Samples
Known GenesUSP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917431
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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