A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766030



Internal ID20541890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64989879..64989879hg38UCSC Ensembl
chr4:65855597..65855597hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288165
Samples
Known GenesLOC401134
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766030
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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