A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968675



Internal ID22743610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61137247..61247111hg38UCSC Ensembl
chr6:61990603..62100467hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38109865
hg19109865
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433984
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968675
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer