A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959278



Internal ID22734314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11262940..11262940hg38UCSC Ensembl
chr10:11304903..11304903hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352454
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959278
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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