A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216989



Internal ID20784029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163634459..163721287hg38UCSC Ensembl
chr6:164055491..164142319hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3886829
hg1986829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216989
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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