A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216782



Internal ID20783822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108074201..108075500hg38UCSC Ensembl
chr6:108395405..108396704hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604373
Supporting Variants
Samples
Known GenesOSTM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216782
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00019


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