A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766081



Internal ID20541941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120687968..120687968hg38UCSC Ensembl
chrX:119821823..119821823hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766081
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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