A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976312



Internal ID22751247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11286060..11596533hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38310474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1355n209
Supporting Variantsnssv17401651
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976312
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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