A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976753



Internal ID22751688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77155274..77261494hg38UCSC Ensembl
chr15:77447616..77553836hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38106221
hg19106221
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370021
Samples
Known GenesLINC00597, PEAK1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976753
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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