A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5674874



Internal ID21701195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6874693..6874693hg38UCSC Ensembl
chr1:6934753..6934753hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17203588, nssv17212647
Samples
Known GenesCAMTA1
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)nsv5674874
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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