A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064806



Internal ID21974039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42900144..42900144hg38UCSC Ensembl
chr8:42755287..42755287hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg383122
hg193122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588943
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064806
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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