A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638176



Internal ID21586481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80679396..80679396hg38UCSC Ensembl
chr8:81591631..81591631hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149274
SamplesNA19983
Known GenesZNF704
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638176
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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