A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641830



Internal ID21590135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92894466..92894466hg38UCSC Ensembl
chr9:95656748..95656748hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163258
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641830
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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