A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030379



Internal ID21939722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16389637..16415186hg38UCSC Ensembl
chr12:16542571..16568120hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3825550
hg1925550
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030379
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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