A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17190938



Internal ID21638447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50820682..50820682hg38UCSC Ensembl
chr12:51214465..51214465hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5704116
Supporting Variants
Samples
Known GenesATF1
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)nssv17190938
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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