A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078903



Internal ID21988136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134327013..134327013hg38UCSC Ensembl
chr4:135248168..135248168hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551812
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078903
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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