A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848261



Internal ID22623196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102855181..102871240hg38UCSC Ensembl
chr10:104614938..104630997hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3816060
hg1916060
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456569
Samples
Known GenesAS3MT, C10orf32, C10orf32-ASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848261
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