A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641416



Internal ID21589721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96083440..96083440hg38UCSC Ensembl
chr7:95712752..95712752hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144592
SamplesHG03125
Known GenesDYNC1I1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641416
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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