A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216498



Internal ID20783538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102353685..102356090hg38UCSC Ensembl
chr6:102801560..102803965hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg382406
hg192406
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216498
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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