A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17238795



Internal ID21686304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62990609..62990609hg38UCSC Ensembl
chr15:63282808..63282808hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5726303
Supporting Variants
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)nssv17238795
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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