A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110261



Internal ID22019494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105981830..105983544hg38UCSC Ensembl
chrX:105225821..105227535hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg381715
hg191715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110261
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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