A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640614



Internal ID21588919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63037870..63037870hg38UCSC Ensembl
chr9:66942842..66942842hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162582
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640614
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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