A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166930



Internal ID21406695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25929822..25930155hg38UCSC Ensembl
chrX:25947939..25948272hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669335
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166930
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