A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155395



Internal ID21511766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43005290..43005290hg38UCSC Ensembl
chr8:42860433..42860433hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635543
Supporting Variants
SamplesNA24385
Known GenesHOOK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155395
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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