A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738103



Internal ID161769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154102987..154103038hg38UCSC Ensembl
chrX:153368439..153368490hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562600
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738103
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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