A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142639



Internal ID21460779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19865582..19865582hg38UCSC Ensembl
chr8:19723093..19723093hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636384
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142639
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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