A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216799



Internal ID20783839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109794943..109825218hg38UCSC Ensembl
chr6:110116146..110146421hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3830276
hg1930276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607500
Supporting Variants
Samples
Known GenesFIG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216799
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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