A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735284



Internal ID20511226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73004913..73004974hg38UCSC Ensembl
chr3:73054064..73054125hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271210
Samples
Known GenesPPP4R2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735284
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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