A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998853



Internal ID21908196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14370415..14371873hg38UCSC Ensembl
chr5:14370524..14371982hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381459
hg191459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555255
Samples
Known GenesTRIO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998853
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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