A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17164863



Internal ID21467155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107274225..107274288hg38UCSC Ensembl
chrX:106517455..106517518hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665884
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17164863
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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