A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976763



Internal ID22751698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33796601..33979181hg38UCSC Ensembl
chr9:33796599..33979179hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38182581
hg19182581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448258
Samples
Known GenesPRSS3, SNORD121A, SNORD121B, UBAP2, UBE2R2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976763
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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