A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998611



Internal ID21907954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8074126..8176434hg38UCSC Ensembl
chr4:8075853..8178161hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38102309
hg19102309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550086
Samples
Known GenesABLIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998611
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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