A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572381



Internal ID20945452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:23409558..23625585hg38UCSC Ensembl
chr5:23409667..23625694hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg38216028
hg19216028
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269448
Samples
Known GenesPRDM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572381
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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