A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417633



Internal ID196824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:83510583..83510686hg38UCSC Ensembl
chrX:82765591..82765694hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417633
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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