A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079875



Internal ID21989108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51854742..51854742hg38UCSC Ensembl
chr3:51888758..51888758hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079875
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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