A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428651



Internal ID207513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80832740..80919484hg38UCSC Ensembl
chrX:80088239..80174983hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3886745
hg1986745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741007
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428651
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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