A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742004



Internal ID20517983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58248663..58248729hg38UCSC Ensembl
chr14:58715381..58715447hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293302
Samples
Known GenesPSMA3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742004
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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