A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv567n206



Internal ID22755871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52729136..52968964hg38UCSC Ensembl
chrX:52758123..52998153hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38239829
hg19240031
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6138355, nsv5422660
Samples
Known GenesFAM156A, FAM156B, SPANXN5, SSX2, SSX2B, XAGE3, XAGE5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv567n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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