A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17200233



Internal ID21647742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35356103..35356103hg38UCSC Ensembl
chr17:33683122..33683122hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5695480
Supporting Variants
Samples
Known GenesSLFN11
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)nssv17200233
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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