A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17114026



Internal ID21503174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3448578..3448578hg38UCSC Ensembl
chr2:3452349..3452349hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg381287
hg191287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614069
Supporting Variants
SamplesNA19239
Known GenesTRAPPC12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17114026
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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