A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166516



Internal ID21483869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152719149..152719485hg38UCSC Ensembl
chrX:151887638..151887974hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672244
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166516
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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