A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428836



Internal ID207694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92129374..92133447hg38UCSC Ensembl
chrX:91384373..91388446hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg384074
hg194074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741449
Samples
Known GenesPCDH11X
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428836
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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