A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366602



Internal ID21024155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186825719..187039187hg38UCSC Ensembl
chr3:186543508..186756975hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38213469
hg19213468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212218
Samples
Known GenesADIPOQ, ADIPOQ-AS1, ST6GAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366602
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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