A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426608



Internal ID205537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153666005..153666129hg38UCSC Ensembl
chrX:152931460..152931584hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426608
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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