A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv580n206



Internal ID22755884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140678368..140689497hg38UCSC Ensembl
chrX:139760533..139771662hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3811130
hg1911130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6138244, nsv5419806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv580n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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