A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17248712



Internal ID21696221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14194620..14194620hg38UCSC Ensembl
chr3:14236120..14236120hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5722751
Supporting Variants
Samples
Known GenesLSM3
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)nssv17248712
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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