A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669757



Internal ID21618062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49689944..49690111hg38UCSC Ensembl
chrX:49454547..49454714hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167437
SamplesHG00513
Known GenesPAGE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669757
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