A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053359



Internal ID21962592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144923007..144923007hg38UCSC Ensembl
chrX:144004527..144004527hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053359
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer