A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192947



Internal ID20759987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24443399..24444655hg38UCSC Ensembl
chr16:24454720..24455976hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381257
hg191257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192947
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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