A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220189



Internal ID20787229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41969667..41970270hg38UCSC Ensembl
chr6:41937405..41938008hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408287
Supporting Variants
Samples
Known GenesCCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220189
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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