A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947128



Internal ID22722630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86337513..86338284hg38UCSC Ensembl
chr16:86371119..86371890hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374684
Samples
Known GenesLINC00917
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947128
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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