A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17188536



Internal ID21636045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50548883..50548883hg38UCSC Ensembl
chr10:52308643..52308643hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5697185
Supporting Variants
Samples
Known GenesSGMS1
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)nssv17188536
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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