A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425476



Internal ID204438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66930000..66949000hg38UCSC Ensembl
chrX:66149842..66168842hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3819001
hg1919001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425476
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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