A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067548



Internal ID21467435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116433604..116433888hg38UCSC Ensembl
chr10:118193116..118193400hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589281
Supporting Variants
SamplesHG03065
Known GenesPNLIPRP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067548
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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