A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv556n206



Internal ID22755860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1157397..1305852hg38UCSC Ensembl
chrX:1257550..1424745hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38148456
hg19167196
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5429811, nsv5430821
Samples
Known GenesCRLF2, CSF2RA, MIR3690, MIR3690-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv556n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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