A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029058



Internal ID21938401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11785833..11785918hg38UCSC Ensembl
chr16:11879689..11879774hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605773
Samples
Known GenesZC3H7A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029058
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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