A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979550



Internal ID22754485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:89142499..90027172hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38884674
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1165n209
Supporting Variantsnssv17403367
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979550
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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