A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289840



Internal ID20499058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:23526846..23527014hg38UCSC Ensembl
chr5:23526955..23527123hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743414
Supporting Variants
Samples
Known GenesPRDM9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289840
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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