A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194073



Internal ID20761113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25358358..26257358hg38UCSC Ensembl
chr16:25369679..26268679hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38899001
hg19899001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507861
Supporting Variants
Samples
Known GenesHS3ST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194073
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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