A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736991



Internal ID160657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52488964..52502964hg38UCSC Ensembl
chrX:52232107..52245359hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3814001
hg1913253
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417824
Supporting Variants
Samples
Known GenesXAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736991
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.47133


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