A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17196008



Internal ID21643517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25935641..25935641hg38UCSC Ensembl
chr15:26180788..26180788hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5713022
Supporting Variants
Samples
Known GenesLOC100128714
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)nssv17196008
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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