A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636660



Internal ID21584965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121143037..121143037hg38UCSC Ensembl
chr8:122155277..122155277hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153407
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636660
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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