A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065485



Internal ID21974718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151678629..151678629hg38UCSC Ensembl
chr4:152599781..152599781hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538151
Samples
Known GenesPET112
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065485
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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