A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203852



Internal ID20770892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12046801..12061900hg38UCSC Ensembl
chr1:142567802..142582894hg19UCSC Ensembl
Cytoband1q12
Allele length
AssemblyAllele length
hg3815100
hg1915093
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203852
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.15828


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