A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738156



Internal ID161822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154839751..154839802hg38UCSC Ensembl
chrX:154068026..154068077hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560081
Supporting Variants
Samples
Known GenesF8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738156
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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