A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640884



Internal ID21589189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186433238..186433238hg38UCSC Ensembl
chr4:187354392..187354392hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126508
SamplesHG00513
Known GenesF11-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640884
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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