A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752153



Internal ID20528013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:29784197..29784197hg38UCSC Ensembl
chr5:29784304..29784304hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752153
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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