A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925366



Internal ID21345436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54325450..54325450hg38UCSC Ensembl
chr4:55191617..55191617hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200335
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925366
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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