A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765254



Internal ID20541114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134959701..134959701hg38UCSC Ensembl
chrX:134093731..134093731hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765254
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