A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033918



Internal ID21943261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25021342..25021410hg38UCSC Ensembl
chr16:25032663..25032731hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033918
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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