A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107397



Internal ID22016630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25211067..25211136hg38UCSC Ensembl
chrX:25229184..25229253hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649146
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107397
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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