A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614638



Internal ID21562943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62120361..62120361hg38UCSC Ensembl
chr3:62106035..62106035hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133683
SamplesHG00732
Known GenesPTPRG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614638
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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