A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628649



Internal ID21576954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109758713..109758713hg38UCSC Ensembl
chr8:110770942..110770942hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159421
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628649
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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