A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667627



Internal ID21615932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46935144..46936228hg38UCSC Ensembl
chrX:46794579..46795663hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg381085
hg191085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167588
SamplesNA19238
Known GenesJADE3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667627
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