A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420730



Internal ID199825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103001918..103012746hg38UCSC Ensembl
chrX:102256846..102267674hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3810829
hg1910829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420730
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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