A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190550



Internal ID20757590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107072511..107077955hg38UCSC Ensembl
chr12:107466289..107471733hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg385445
hg195445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456704
Supporting Variants
Samples
Known GenesCRY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190550
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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