A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629759



Internal ID21578064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81067609..81067609hg38UCSC Ensembl
chr8:81979844..81979844hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143080
SamplesNA19238
Known GenesPAG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629759
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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