A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv577n206



Internal ID22755881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109556727..109556900hg38UCSC Ensembl
chrX:108799956..108800129hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5416854, nsv5416835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv577n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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