A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428203



Internal ID207082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1628109..1714900hg38UCSC Ensembl
chrX:1747002..1833793hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3886792
hg1986792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738881
Samples
Known GenesASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428203
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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