A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037633



Internal ID21946976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48181266..48181579hg38UCSC Ensembl
chr16:48215177..48215490hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632193
Samples
Known GenesABCC11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037633
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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