A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939255



Internal ID22714645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11237946..11238850hg38UCSC Ensembl
chr16:11331803..11332707hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939255
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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