A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971077



Internal ID22746012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131313928..131644148hg38UCSC Ensembl
chr12:131798473..132128693hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38330221
hg19330221
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361721
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971077
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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