A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736989



Internal ID160655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52451703..52541422hg38UCSC Ensembl
chrX:52194846..52570432hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3889720
hg19375587
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562458
Supporting Variants
Samples
Known GenesXAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736989
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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