A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431883



Internal ID210647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:106300051..106441723hg38UCSC Ensembl
chrX:105543267..105684953hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38141673
hg19141687
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431883
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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