A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641067



Internal ID21589372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6457169..6457169hg38UCSC Ensembl
chr7:6496800..6496800hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157323
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641067
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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