A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280488



Internal ID20489706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46747868..46748009hg38UCSC Ensembl
chr4:46749885..46750026hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744960
Supporting Variants
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280488
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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