A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032645



Internal ID21941988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58248679..58248755hg38UCSC Ensembl
chr14:58715397..58715473hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617521
Samples
Known GenesPSMA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032645
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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