A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855035



Internal ID22629970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79526084..79533089hg38UCSC Ensembl
chr10:81285840..81292845hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387006
hg197006
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855035
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