A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067784



Internal ID21977017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52617576..52617576hg38UCSC Ensembl
chr3:52651592..52651592hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550752
Samples
Known GenesPBRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067784
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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