A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038143



Internal ID21947486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1738357..1738444hg38UCSC Ensembl
chr16:1788358..1788445hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614093
Samples
Known GenesMAPK8IP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038143
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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