A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166300



Internal ID21500279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154831507..154831781hg38UCSC Ensembl
chrX:154059782..154060056hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666602
Supporting Variants
SamplesNA19239
Known GenesSMIM9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166300
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