A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17181404



Internal ID21628913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35426962..35426962hg38UCSC Ensembl
chr7:35466572..35466572hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5683647
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)nssv17181404
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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