A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372724



Internal ID22598393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95689918..95691490hg38UCSC Ensembl
chr15:96233147..96234719hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381573
hg191573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372724
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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