A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752264



Internal ID20528124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151166577..151166577hg38UCSC Ensembl
chr5:150546138..150546138hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg382294
hg192294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752264
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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