A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629108



Internal ID21577413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:320859..320859hg38UCSC Ensembl
chr9:320859..320859hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161943, nssv17161942
SamplesHG03125, NA24385
Known GenesDOCK8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629108
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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