A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5698094



Internal ID21724415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64079130..64079130hg38UCSC Ensembl
chr17:62156490..62156490hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17198461, nssv17232181
Samples
Known GenesERN1
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)nsv5698094
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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