A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198844



Internal ID20765884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44522346..44537314hg38UCSC Ensembl
chr19:45026375..45041301hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3814969
hg1914927
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532465
Supporting Variants
Samples
Known GenesCEACAM20, CEACAM22P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198844
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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