A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619885



Internal ID21568190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9270952..9270952hg38UCSC Ensembl
chrX:9238992..9238992hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169086
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619885
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