A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971832



Internal ID22746767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25064145..25077276hg38UCSC Ensembl
chr6:25064373..25077504hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3813132
hg1913132
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446484
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971832
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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