A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931641



Internal ID22706928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4950495..4954611hg38UCSC Ensembl
chr16:5000496..5004612hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384117
hg194117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376535
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931641
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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