A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17252786



Internal ID21700295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3054573..3054573hg38UCSC Ensembl
chr6:3054807..3054807hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5723345
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)nssv17252786
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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