A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222643



Internal ID20789683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33827389..33879295hg38UCSC Ensembl
chr6:33795166..33847072hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3851907
hg1951907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407836
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222643
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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