A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032881



Internal ID21942224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119434151..119435265hg38UCSC Ensembl
chr11:119304861..119305975hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381115
hg191115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612697
Samples
Known GenesUSP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032881
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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