A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947388



Internal ID22722893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85645795..85645851hg38UCSC Ensembl
chr16:85679401..85679457hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372639
Samples
Known GenesGSE1, MIR7851
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947388
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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