A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854112



Internal ID22629047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49646009..49655761hg38UCSC Ensembl
chr13:50220145..50229897hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg389753
hg199753
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv527n209
Supporting Variantsnssv17466444
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854112
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