A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17208987



Internal ID21656496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73859063..73859063hg38UCSC Ensembl
chr2:74086190..74086190hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5687663
Supporting Variants
Samples
Known GenesSTAMBP
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)nssv17208987
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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