A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633363



Internal ID21581668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14374819..14374819hg38UCSC Ensembl
chr10:14416818..14416818hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069179
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633363
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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