A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627357



Internal ID21575662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1435499..1435499hg38UCSC Ensembl
chr10:1477694..1477694hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069178
SamplesHG02818
Known GenesADARB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627357
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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