A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763166



Internal ID20539026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:78650931..78655345hg38UCSC Ensembl
chrX:77906428..77910842hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg384415
hg194415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763166
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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