A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17200298



Internal ID21647807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39443812..39443812hg38UCSC Ensembl
chr17:37600065..37600065hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5700384
Supporting Variants
Samples
Known GenesMED1
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)nssv17200298
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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