A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744960



Internal ID20520964
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 StatusM
Merged Variants
Supporting Variantsnssv16280488
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744960
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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