A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17203547



Internal ID21651056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138268399..138268399hg38UCSC Ensembl
chrX:137350558..137350558hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5716607
Supporting Variants
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17203547
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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