A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931985



Internal ID22707277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89829649..89831981hg38UCSC Ensembl
chr16:89896057..89898389hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382333
hg192333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377120
Samples
Known GenesSPIRE2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931985
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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