A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5677526



Internal ID21703847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205255715..205255715hg38UCSC Ensembl
chr1:205224843..205224843hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17188680, nssv17207019
Samples
Known GenesTMCC2
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)nsv5677526
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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