A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866772



Internal ID22641707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92115852..92132282hg38UCSC Ensembl
chr13:92768105..92784535hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3816431
hg1916431
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468236
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866772
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