A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5678956



Internal ID21705277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9993600..9993600hg38UCSC Ensembl
chr2:10133728..10133728hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17196887
Samples
Known GenesGRHL1
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)nsv5678956
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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