A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17239731



Internal ID21687240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38345031..38345031hg38UCSC Ensembl
chr13:38919168..38919168hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5730736
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)nssv17239731
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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