A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732624



Internal ID20508548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132744899..132744954hg38UCSC Ensembl
chr11:132614794..132614849hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282288
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732624
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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