A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17244513



Internal ID21692022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17647293..17647293hg38UCSC Ensembl
chrX:17665413..17665413hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5721971
Supporting Variants
Samples
Known GenesNHS
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)nssv17244513
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