A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17188487



Internal ID21635996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28272826..28272826hg38UCSC Ensembl
chr10:28561755..28561755hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5705180
Supporting Variants
Samples
Known GenesMPP7
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)nssv17188487
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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