A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616936



Internal ID21565241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82071184..82071184hg38UCSC Ensembl
chr3:82120335..82120335hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127297
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616936
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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