A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855334



Internal ID22630269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49238660..49241697hg38UCSC Ensembl
chr12:49632443..49635480hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg383038
hg193038
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460221
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855334
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