A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626012



Internal ID21574317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108000368..108000368hg38UCSC Ensembl
chr9:110762649..110762649hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157531
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626012
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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