A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895442



Internal ID22670524
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 StatusM
Merged Variants
Supporting Variantsnssv17411205
Samples
Known GenesPRDM9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895442
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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