A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025524



Internal ID21934867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2833452..2833734hg38UCSC Ensembl
chr16:2883453..2883735hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601519
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025524
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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