A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940402



Internal ID22715811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81516912..81517251hg38UCSC Ensembl
chr16:81550517..81550856hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372347
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940402
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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