A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069733



Internal ID21978966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143630227..143630227hg38UCSC Ensembl
chr6:143951364..143951364hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575684
Samples
Known GenesPHACTR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069733
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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