A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629476



Internal ID21577781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38729142..38729142hg38UCSC Ensembl
chr9:38729139..38729139hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162211
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629476
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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