A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17214880



Internal ID21662389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44296846..44296846hg38UCSC Ensembl
chr7:44336445..44336445hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5676434
Supporting Variants
Samples
Known GenesCAMK2B
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)nssv17214880
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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