A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739805



Internal ID20515781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23365289..23365458hg38UCSC Ensembl
chr16:23376610..23376779hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290637
Samples
Known GenesSCNN1B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739805
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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