A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5714358



Internal ID21740679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8699644..8699644hg38UCSC Ensembl
chr12:8852240..8852240hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17235420
Samples
Known GenesRIMKLB
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)nsv5714358
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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