A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605876



Internal ID21554181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3800531..3800531hg38UCSC Ensembl
chr3:3842215..3842215hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124370
SamplesHG03486
Known GenesLRRN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605876
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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