A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607861



Internal ID21556166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86135662..86135662hg38UCSC Ensembl
chr3:86184812..86184812hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg386095
hg196095
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123365
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607861
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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