A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932717



Internal ID22708020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29237177..29237226hg38UCSC Ensembl
chr16:29248498..29248547hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932717
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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