A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134466



Internal ID21456699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38064668..38064668hg38UCSC Ensembl
chr3:38106159..38106159hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623360
Supporting Variants
SamplesHG02587
Known GenesDLEC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134466
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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