A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110353



Internal ID22019586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103523960..103524079hg38UCSC Ensembl
chrX:102778888..102779007hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110353
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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