A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431007



Internal ID209796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:93553384..93556783hg38UCSC Ensembl
chrX:92808383..92811782hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431007
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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