A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930581



Internal ID22705850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27064186..27064239hg38UCSC Ensembl
chr16:27075507..27075560hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930581
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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