A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17237401



Internal ID21684910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36222848..36222848hg38UCSC Ensembl
chr19:36713750..36713750hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5728222
Supporting Variants
Samples
Known GenesZNF146
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)nssv17237401
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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