A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618631



Internal ID21566936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13147547..13147547hg38UCSC Ensembl
chr4:13149171..13149171hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382470
hg192470
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134760
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618631
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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