A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613055



Internal ID21561360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149108651..149108651hg38UCSC Ensembl
chrX:148190181..148190181hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166263
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613055
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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