A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642314



Internal ID21590619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74941846..74941846hg38UCSC Ensembl
chr8:75854081..75854081hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144159
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642314
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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