A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378623



Internal ID22436493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84919264..84928423hg38UCSC Ensembl
chr15:85462495..85471654hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg389160
hg199160
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968316
Supporting Variants
Samples
Known GenesSLC28A1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378623
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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