A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611897



Internal ID21560202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126260396..126260396hg38UCSC Ensembl
chr3:125979239..125979239hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131177
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611897
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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