A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045720



Internal ID21889776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103772857..103772857hg38UCSC Ensembl
chrX:103027785..103027785hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg383350
hg193350
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045720
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