A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429050



Internal ID207908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39044335..39045109hg38UCSC Ensembl
chrX:38903588..38904362hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736460
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429050
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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