A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972236



Internal ID22747171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84955829..84964833hg38UCSC Ensembl
chr13:85529964..85538968hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg389005
hg199005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388811
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972236
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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