A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5713011



Internal ID21739332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101939624..101939624hg38UCSC Ensembl
chr10:103699381..103699381hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17189321
Samples
Known GenesC10orf76
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5713011
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer