A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202037



Internal ID20769078
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 StatusS
Merged Variantsnsv6332784
Supporting Variants
Samples
Known GenesCELA3A, CELA3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202037
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00081


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