A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417819



Internal ID197008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24093173..24098547hg38UCSC Ensembl
chrX:24111290..24116664hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg385375
hg195375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417819
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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