A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5708974



Internal ID21735295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102082477..102082477hg38UCSC Ensembl
chr12:102476255..102476255hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17217923, nssv17193309
Samples
Known GenesNUP37
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)nsv5708974
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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