A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625076



Internal ID21573381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93116043..93116043hg38UCSC Ensembl
chr10:94875800..94875800hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071557
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625076
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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