A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023011



Internal ID21932354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30005791..30039857hg38UCSC Ensembl
chr16:30017112..30051178hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3834067
hg1934067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630780
Samples
Known GenesC16orf92, DOC2A, FAM57B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023011
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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