A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939184



Internal ID22714573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4635150..4636857hg38UCSC Ensembl
chr16:4685151..4686858hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381708
hg191708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387139
Samples
Known GenesMGRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939184
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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