A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741719



Internal ID20517697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179871733..179871877hg38UCSC Ensembl
chr5:179298733..179298877hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280605
Samples
Known GenesTBC1D9B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741719
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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