A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019882



Internal ID20586922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58254343..58254850hg38UCSC Ensembl
chr14:58721061..58721568hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490753
Supporting Variants
Samples
Known GenesPSMA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00061


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