A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5718737



Internal ID21745058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56279356..56279356hg38UCSC Ensembl
chr12:56673140..56673140hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17251513
Samples
Known GenesCS
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)nsv5718737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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