A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969675



Internal ID22744610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44411583..44413463hg38UCSC Ensembl
chr13:44985719..44987599hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376895
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969675
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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