A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744065



Internal ID20520060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183711669..183711758hg38UCSC Ensembl
chr4:184632822..184632911hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296760
Samples
Known GenesTRAPPC11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744065
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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