A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5726925



Internal ID21753246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17700554..17700554hg38UCSC Ensembl
chr6:17700785..17700785hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17234072
Samples
Known GenesNUP153
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)nsv5726925
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer