A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514778



Internal ID20888133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12917793..12927447hg38UCSC Ensembl
chr16:13011650..13021304hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg389655
hg199655
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180418
Samples
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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