A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766558



Internal ID20542418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155638289..155638343hg38UCSC Ensembl
chrX:154867950..154868004hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766558
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