A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862417



Internal ID22637352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77478401..77480100hg38UCSC Ensembl
chr13:78052536..78054235hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862417
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