A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736900



Internal ID160566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49530394..49604394hg38UCSC Ensembl
chrX:49294997..49368997hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3874001
hg1974001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421860
Supporting Variants
Samples
Known GenesGAGE1, GAGE12B, GAGE12C, GAGE12D, GAGE12E, GAGE12F, GAGE12G, GAGE12H, GAGE12I, GAGE2A, GAGE2E, GAGE6, GAGE8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736900
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.381985


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