A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079878



Internal ID21989111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41121856..41121856hg38UCSC Ensembl
chr4:41123873..41123873hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537715
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079878
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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