A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17238747



Internal ID21686256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33013845..33013845hg38UCSC Ensembl
chr13:33587983..33587983hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5721756
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)nssv17238747
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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