A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934864



Internal ID22710196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4580861..4598089hg38UCSC Ensembl
chr16:4630862..4648090hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3817229
hg1917229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389510
Samples
Known GenesC16orf96
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934864
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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