A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863242



Internal ID22638177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91575751..91578967hg38UCSC Ensembl
chr12:91969528..91972744hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg383217
hg193217
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863242
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