A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5723573



Internal ID21749894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76117392..76117392hg38UCSC Ensembl
chr11:75828436..75828436hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17244944
Samples
Known GenesUVRAG
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)nsv5723573
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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