A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411205



Internal ID22469075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:23527621..23572869hg38UCSC Ensembl
chr5:23527730..23572978hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3845249
hg1945249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895442
Supporting Variants
Samples
Known GenesPRDM9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411205
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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