A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905580



Internal ID22680768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186850021..186860031hg38UCSC Ensembl
chr3:186567810..186577820hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3810011
hg1910011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413463
Samples
Known GenesADIPOQ, ADIPOQ-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905580
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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