A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613973



Internal ID21562278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32002687..32002687hg38UCSC Ensembl
chr3:32044179..32044179hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128874
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613973
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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