A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637997



Internal ID21586302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1850724..1850724hg38UCSC Ensembl
chr9:1850724..1850724hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161384
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637997
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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