A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217072



Internal ID20784112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148153905..148154332hg38UCSC Ensembl
chr6:148475041..148475468hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607164
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217072
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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