A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17246015



Internal ID21693524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63821050..63821050hg38UCSC Ensembl
chr11:63588522..63588522hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5723354
Supporting Variants
Samples
Known GenesC11orf84
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a SVA mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17246015
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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