A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159065



Internal ID21478685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102601986..102601986hg38UCSC Ensembl
chr8:103614214..103614214hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633806
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159065
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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