A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17236450



Internal ID21683959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38584903..38584903hg38UCSC Ensembl
chrX:38444156..38444156hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5728559
Supporting Variants
Samples
Known GenesTSPAN7
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)nssv17236450
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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