A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5714935



Internal ID21741256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96739097..96739097hg38UCSC Ensembl
chr10:98498854..98498854hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17250922
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)nsv5714935
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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