A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588943



Internal ID21780986
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 StatusS
Merged Variantsnsv6064806
Supporting Variants
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588943
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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