A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413463



Internal ID22471333
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 StatusS
Merged Variantsnsv5905580
Supporting Variants
Samples
Known GenesADIPOQ, ADIPOQ-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413463
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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