A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971444



Internal ID22746379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102031291..102091442hg38UCSC Ensembl
chr4:102952448..103012599hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3860152
hg1960152
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410671
Samples
Known GenesBANK1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971444
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