A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631786



Internal ID21580091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108247879..108247879hg38UCSC Ensembl
chr9:111010159..111010159hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151849
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631786
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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