A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233447



Internal ID20800487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23379017..23432128hg38UCSC Ensembl
chr6:23379245..23432356hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3853112
hg1953112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233447
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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