A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048307



Internal ID21957540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41211776..41211776hg38UCSC Ensembl
chrX:41071029..41071029hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644210
Samples
Known GenesUSP9X
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048307
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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