A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202047



Internal ID20769088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21999189..22063090hg38UCSC Ensembl
chr1:22325682..22389583hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3863902
hg1963902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319052
Supporting Variants
Samples
Known GenesCDC42, CELA3A, LINC00339
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202047
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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