A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635304



Internal ID21583609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102254775..102254775hg38UCSC Ensembl
chr10:104014532..104014532hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067470
SamplesHG03009
Known GenesGBF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635304
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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