A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17249255



Internal ID21696764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65884213..65884213hg38UCSC Ensembl
chr11:65651684..65651684hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5723155
Supporting Variants
Samples
Known GenesFIBP
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)nssv17249255
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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