A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060867



Internal ID21970100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121855938..121855938hg38UCSC Ensembl
chr4:122777093..122777093hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543675
Samples
Known GenesBBS7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060867
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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