A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138659



Internal ID337843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:69448000..69477000hg38UCSC Ensembl
chrX:68667843..68696843hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3829001
hg1929001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138659
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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