A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411566



Internal ID21069119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23379017..23432128hg38UCSC Ensembl
chr6:23379245..23432356hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3853112
hg1953112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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