A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030267



Internal ID21939610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74372145..74443308hg38UCSC Ensembl
chr16:74406043..74477206hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3871164
hg1971164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624423
Samples
Known GenesCLEC18B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030267
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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