A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5723991



Internal ID21750312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51778312..51778312hg38UCSC Ensembl
chr20:50394851..50394851hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17251914
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)nsv5723991
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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