A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027073



Internal ID21936416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3288225..3310121hg38UCSC Ensembl
chr16:3338225..3360121hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3821897
hg1921897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616687
Samples
Known GenesTIGD7, ZNF263, ZNF75A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027073
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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