A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv583n206



Internal ID22755887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:142755281..142774054hg38UCSC Ensembl
chrX:141843067..141861840hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3818774
hg1918774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5416945, nsv5420404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv583n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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