A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332784



Internal ID20865959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21986170..22009038hg38UCSC Ensembl
chr1:22312663..22335531hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3822869
hg1922869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv114n223
Supporting Variantsnssv18202037
Samples
Known GenesCELA3A, CELA3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332784
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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