A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641971



Internal ID21590276
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 StatusM
Merged Variants
Supporting Variantsnssv17150009
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641971
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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