A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050764



Internal ID21959997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41988259..41988259hg38UCSC Ensembl
chrX:41847512..41847512hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg382040
hg192040
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050764
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