A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5552429



Internal ID325787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153405987..153405987hg38UCSC Ensembl
chrX:152671445..152671445hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5552429
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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