A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945198



Internal ID22720672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12906758..12907013hg38UCSC Ensembl
chr16:13000615..13000870hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389402
Samples
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945198
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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