A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065415



Internal ID21974648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:190122511..190122511hg38UCSC Ensembl
chr4:191043666..191043666hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065415
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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