A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147627



Internal ID21488788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119357989..119357989hg38UCSC Ensembl
chr8:120370229..120370229hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629780
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147627
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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