A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757468



Internal ID20533328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48455242..48455242hg38UCSC Ensembl
chr4:48457259..48457259hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757468
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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