A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5723654



Internal ID21749975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37817186..37817186hg38UCSC Ensembl
chr22:38213193..38213193hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17240751, nssv17249254
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)nsv5723654
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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