A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738593



Internal ID20514563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28088773..28089338hg38UCSC Ensembl
chr16:28100094..28100659hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738593
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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