A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941127



Internal ID22716546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29168200..29171342hg38UCSC Ensembl
chr16:29179521..29182663hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383143
hg193143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941127
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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