A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032655



Internal ID21941998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1738653..1738723hg38UCSC Ensembl
chr16:1788654..1788724hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610546
Samples
Known GenesMAPK8IP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032655
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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