A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110960



Internal ID22020193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92099709..92107102hg38UCSC Ensembl
chrX:91354708..91362101hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg387394
hg197394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639651
Samples
Known GenesPCDH11X
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110960
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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