A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968293



Internal ID22743229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118089140..118089735hg38UCSC Ensembl
chr12:118526945..118527540hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367743
Samples
Known GenesVSIG10
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968293
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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