A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667006



Internal ID21615312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105826224..105826283hg38UCSC Ensembl
chrX:105070217..105070276hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165218
SamplesNA20509
Known GenesNRK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667006
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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