A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939043



Internal ID22714431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11471997..11472091hg38UCSC Ensembl
chr16:11565853..11565947hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939043
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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