A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17234434



Internal ID21681943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93256339..93256339hg38UCSC Ensembl
chr1:93721896..93721896hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5726944
Supporting Variants
Samples
Known GenesCCDC18
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)nssv17234434
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