A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293647



Internal ID20502865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14638507..14638583hg38UCSC Ensembl
chr11:14660053..14660129hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737152
Supporting Variants
Samples
Known GenesPSMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293647
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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