A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082649



Internal ID21509424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36173578..36173578hg38UCSC Ensembl
chr14:36642784..36642784hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652705
Supporting Variants
SamplesNA20847
Known GenesPTCSC3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082649
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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