A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613991



Internal ID21562296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93635279..93635279hg38UCSC Ensembl
chr1:94100835..94100835hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068252
SamplesHG03125
Known GenesBCAR3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613991
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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