A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636995



Internal ID21585300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80699426..80699426hg38UCSC Ensembl
chr8:81611661..81611661hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149594
SamplesHG03683
Known GenesZNF704
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636995
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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