A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17252885



Internal ID21700394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9730060..9730060hg38UCSC Ensembl
chr3:9771744..9771744hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5716653
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)nssv17252885
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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