A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928226



Internal ID21348295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63688218..63688218hg38UCSC Ensembl
chr6:64398119..64398119hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202501
SamplesHG002
Known GenesPHF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928226
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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