A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045303



Internal ID21954571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65538493..65538493hg38UCSC Ensembl
chrX:64758373..64758373hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045303
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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