A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963274



Internal ID22738209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45579431..45579431hg38UCSC Ensembl
chr10:46074879..46074879hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363893
Samples
Known GenesMARCH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963274
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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