A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968894



Internal ID22743829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131246524..131248082hg38UCSC Ensembl
chr5:130582217..130583775hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg381559
hg191559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417270
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968894
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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