A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077598



Internal ID21986831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119014652..119014652hg38UCSC Ensembl
chr4:119935807..119935807hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552355
Samples
Known GenesSYNPO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077598
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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