A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980223



Internal ID22755158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26652285..26661265hg38UCSC Ensembl
chr1:26978776..26987756hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388981
hg198981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367349
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980223
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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