A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421093



Internal ID200181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27947016..27959951hg38UCSC Ensembl
chrX:27965133..27978068hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3812936
hg1912936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421093
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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