A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069766



Internal ID21978999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62277182..62277182hg38UCSC Ensembl
chr3:62262857..62262857hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546008
Samples
Known GenesPTPRG, PTPRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069766
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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