A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972810



Internal ID22747745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:36768687..38268951hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381500265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n209
Supporting Variantsnssv17376738
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972810
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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