A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105967



Internal ID22015200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:126154409..126186251hg38UCSC Ensembl
chrX:125288392..125320234hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3831843
hg1931843
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649734
Samples
Known GenesDCAF12L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105967
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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