A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627682



Internal ID21575987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67831114..67831114hg38UCSC Ensembl
chr8:68743349..68743349hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154238
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627682
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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