A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946671



Internal ID22722165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27827887..27827945hg38UCSC Ensembl
chr16:27839208..27839266hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387410
Samples
Known GenesGSG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946671
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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