A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640223



Internal ID21588528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84019549..84019549hg38UCSC Ensembl
chr6:84729268..84729268hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157552
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640223
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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