A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150009



Internal ID21457029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98371987..98371987hg38UCSC Ensembl
chr8:99384215..99384215hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg386227
hg196227
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641971
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150009
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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