A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17247403



Internal ID21694912
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 StatusS
Merged Variantsnsv5715370
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)nssv17247403
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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