A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023832



Internal ID21933175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3330405..3350057hg38UCSC Ensembl
chr16:3380405..3400057hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819653
hg1919653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023832
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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