A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv572n206



Internal ID22755876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76903108..76927435hg38UCSC Ensembl
chrX:76123533..76147860hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3824328
hg1924328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5423083, nsv5431237
Samples
Known GenesMIR384
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv572n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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