A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951939



Internal ID22727277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102293768..102293768hg38UCSC Ensembl
chr10:104053525..104053525hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360948
Samples
Known GenesGBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951939
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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