A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17213862



Internal ID21661371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92092457..92092457hg38UCSC Ensembl
chr7:91721771..91721771hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5680498
Supporting Variants
Samples
Known GenesAKAP9
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)nssv17213862
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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