A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642399



Internal ID21590704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117132236..117132236hg38UCSC Ensembl
chr6:117453399..117453399hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142548
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642399
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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