A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019860



Internal ID21929203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82259928..82265808hg38UCSC Ensembl
chr6:82969645..82975525hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385881
hg195881
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019860
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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