A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941717



Internal ID22717146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24250437..24251916hg38UCSC Ensembl
chr16:24261758..24263237hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381480
hg191480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941717
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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