A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504153



Internal ID20877414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27369462..27370239hg38UCSC Ensembl
chr16:27380783..27381560hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504153
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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