A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429792



Internal ID208627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52374717..52375089hg38UCSC Ensembl
chrX:52117860..52118232hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736984
Samples
Known GenesXAGE2, XAGE2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429792
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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