A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733280



Internal ID20509208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185740595..185740776hg38UCSC Ensembl
chr4:186661749..186661930hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264522
Samples
Known GenesSORBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733280
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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