A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060773



Internal ID21970006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146104185..146104185hg38UCSC Ensembl
chr4:147025337..147025337hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060773
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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