A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv563n206



Internal ID22755867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8465488..8805488hg38UCSC Ensembl
chrX:8433529..8773529hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38340001
hg19340001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5431771, nsv5429354
Samples
Known GenesFAM9A, KAL1, VCX3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv563n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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