A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624509



Internal ID21572814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2841710..2841710hg38UCSC Ensembl
chrX:2759751..2759751hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166758
SamplesHG01505
Known GenesGYG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624509
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