A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238274



Internal ID20805314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40725804..40726544hg38UCSC Ensembl
chr15:41018002..41018742hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576234
Supporting Variants
Samples
Known GenesRAD51
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238274
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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