A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752567



Internal ID20528427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1568665..1568665hg38UCSC Ensembl
chr4:1570392..1570392hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752567
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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