A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5675507



Internal ID21701828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72957973..72957973hg38UCSC Ensembl
chr3:73007124..73007124hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17215834
Samples
Known GenesGXYLT2
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)nsv5675507
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