A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223437



Internal ID20790477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:67206232..67301596hg38UCSC Ensembl
chr6:67916125..68011489hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3895365
hg1995365
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223437
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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