A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057467



Internal ID21966700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27632915..27632915hg38UCSC Ensembl
chr3:27674406..27674406hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057467
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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