A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736899



Internal ID160565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49319837..49343837hg38UCSC Ensembl
chrX:49176316..49219304hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3824001
hg1942989
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425583
Supporting Variants
Samples
Known GenesGAGE12F, GAGE12I, GAGE12J, GAGE13, GAGE2A, GAGE2C, GAGE2D, GAGE2E, GAGE4, GAGE5, GAGE7, GAGE8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736899
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.483333


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