A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740526



Internal ID20516502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119358269..119358415hg38UCSC Ensembl
chr11:119228979..119229125hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275840
Samples
Known GenesUSP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740526
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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