A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5715370



Internal ID21741691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73661661..73661661hg38UCSC Ensembl
chr10:75421419..75421419hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381147
hg191147
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17247403
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)nsv5715370
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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