A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072873



Internal ID21982106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186113324..186113324hg38UCSC Ensembl
chr3:185831113..185831113hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072873
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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