A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417659



Internal ID196851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:126994382..126995994hg38UCSC Ensembl
chrX:126128365..126129977hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381613
hg191613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417659
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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