A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5722064



Internal ID21748385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76571684..76571684hg38UCSC Ensembl
chr11:76282728..76282728hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17235100, nssv17238926
Samples
Known Genes
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)nsv5722064
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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