A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979667



Internal ID22754602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24646334..25024564hg38UCSC Ensembl
chr13:25220472..25598702hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38378231
hg19378231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378169
Samples
Known GenesATP12A, CENPJ, RNF17, TPTE2P1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979667
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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