A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625342



Internal ID21573647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101419833..101419833hg38UCSC Ensembl
chr9:104182115..104182115hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145103
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625342
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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