A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023433



Internal ID21932776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51780177..51780233hg38UCSC Ensembl
chr16:51814088..51814144hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023433
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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