A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17219661



Internal ID21667170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22549747..22549747hg38UCSC Ensembl
chr7:22589366..22589366hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5689978
Supporting Variants
Samples
Known Genes
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)nssv17219661
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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