A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101428



Internal ID22010661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76374449..77105512hg38UCSC Ensembl
chrX:75594848..76325925hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38731064
hg19731078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645389
Samples
Known GenesMAGEE1, MIR384
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101428
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer