A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611711



Internal ID21560016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194025276..194025276hg38UCSC Ensembl
chr3:193743065..193743065hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134329
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611711
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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