A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626274



Internal ID21574579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33755682..33755682hg38UCSC Ensembl
chr8:33613200..33613200hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151163
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626274
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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